hawaii5oh
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Post by hawaii5oh on Apr 17, 2018 0:55:13 GMT -5
For Immediate Release April 13, 2018Seacrest Foods Recalls l’Explorateur Soft Ripened Cheese Due to Possible Health RiskSeacrest Foods International, Inc. of Lynn, MA is voluntarily recalling 29 cases of Formagere de la Brie brand, l’Explorateur soft ripened cheese because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, pregnant women and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages, stillbirths and fetal infection among pregnant women. The Formagere de la Brie brand, l’Explorateur, soft ripened cheese made from pasteurized milk, was distributed at retail stores in Connecticut, Massachusetts, Maine, New Jersey and New Hampshire beginning on 02/06/2018 through 03/31/18. The l’Explorateur product comes in a 250g (8.8 oz), clear plastic package marked with lot # H010 or H011 on the bottom, with UPC: 3 390010 004080.No illnesses have been confirmed by public health authorities to date. The cheese was manufactured by Fromagere de la Brie of St. Simeon, France. Seacrest Foods was one of several importers notified by their French Consolidator of a potentially positive test result for Listeria monocytogenes. Seacrest Foods is taking these steps because of our dedication to providing quality foods, and that must start with ensuring the safety of all the food we import and distribute. This recall is being undertaken with the knowledge of the FDA. Consumers should not consume the product, and should discard it or return the product to the store for refund. Seacrest Foods representatives have already been in contact with retail customers that received product directly from their company and requested that they remove the recalled product from store shelves and inventories and that no product is available for consumer purchase. Consumers with questions may contact Seacrest Foods at 781-581-2066 between the hours of 9:00 a.m. and 5 p.m. EST, Monday through Friday. www.fda.gov/Safety/Recalls/ucm604632.htm
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hawaii5oh
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Post by hawaii5oh on Apr 17, 2018 0:58:44 GMT -5
For Immediate Release April 13, 2018K9 Natural Ltd Voluntarily Recalls K9 Natural Frozen Chicken Feast Raw Pet Food 2.2lb And 11lb Bags Because Of Possible Listeria MonocytogenesK9 Natural Ltd is voluntarily recalling four batches of the K9 Natural Frozen Chicken Feast 2.2lb and 11lb bags that was imported into the US market in June 2017 because they have the potential to be contaminated with Listeria Monocytogenes. Listeria Monocytogenes is an organism that can cause serious and sometimes fatal infections in humans and animals. Symptoms of infection may include nausea, vomiting, aches, fever, and diarrhea, and may lead to most serious issues such as meningitis and abortion. Healthy people and animals can be infected, and some are more susceptible, including young children, pregnant women, frail or elderly people or others with weakened immune symptoms. Animals that become ill with Listeria Monocytogenes could display symptoms similar to humans. Listeria Monocytogenes can affect animals eating the product and there is risk to humans from handling the products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to the products. No pet or human illnesses, injuries or complaints have been reported to date. If you have any symptoms after handling the recalled product, please contact your healthcare provider. If your pet has consumed the recalled product and has any symptoms, please contact your veterinarian. The recalled batch numbers are as follows;K9 Natural Frozen Chicken Feast 2.2lb bags, shipped to distributors in WA, CA, TX, CO and distributed to pet speciality retail stores.Batch number #170517 with an expiration date of 17NOV2018
K9 Natural Frozen Chicken Feast 11lb bags, shipped to distributors in WA, CA, TX, CO, PA and distributed to pet speciality retail stores. Batch number #150517 with an expiration date of 15NOV2018 Batch number #160517 with an expiration date of 16NOV2018 Batch number #170517 with an expiration date of 17NOV2018The batch number and expiration dates are stamped in the bottom left on the back of the pack. You can see examples of packaging and where to find the batch number here; Purchasers are encouraged to check the batch code to see if their product was affected. Pet owners who have product matching these batch codes should stop using the product and return the unused portion to the place of purchase for a full refund or replacement. Consumers with questions can contact us at 1 888 345 4680. Customers with questions may contact the company via phone at 1 888 345 4680, M-F 8am-5pm PST & EST and S-S 14 &15 April 2018 8am-5pm PST & EST or email info@k9natural.com. www.fda.gov/Safety/Recalls/ucm604645.htm
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hawaii5oh
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Post by hawaii5oh on Apr 17, 2018 1:03:03 GMT -5
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hawaii5oh
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The sixth sick sheik's sixth sheep's sick.
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Post by hawaii5oh on Apr 17, 2018 2:47:23 GMT -5
For Immediate Release April 13, 2018Rose Acre Farms Recalls Shell Eggs Due to Possible Health RiskThrough an abundance of caution Rose Acre Farms of Seymour, Indiana is voluntarily recalling 206,749,248 eggs because they have the potential to be contaminated with Salmonella Braenderup, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy individuals infected with Salmonella Braenderup can experience fever, diarrhea, nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella Braenderup can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis. The eggs were distributed from the farm in Hyde County, North Carolina and reached consumers in the following states: Colorado, Florida, New Jersey, New York, North Carolina, Pennsylvania, South Carolina, Virginia, and West Virginia through retail stores and restaurants via direct delivery. 22 illnesses have been reported to date. The affected eggs, from plant number P-1065 with the Julian date range of 011 through date of 102 printed on either the side portion or the principal side of the carton or package, as follows: Lot Codes 011 – 102 [click on the link below to view the recalled products] The voluntary recall was a result of some illnesses reported on the U.S. East Coast, which led to extensive interviews and eventually a thorough FDA inspection of the Hyde County farm, which produces 2.3 million eggs a day. The facility includes 3 million laying hens with a USDA inspector on-site daily. Consumers who have purchased shells eggs are urged to immediately discontinue use of the recalled eggs and to return them to the place of purchase for a full refund. Consumers with questions may contact the company at (855) 215-5730 between the hours of 8 a.m. to 5 p.m. Eastern Standard time. www.fda.gov/Safety/Recalls/ucm604640.htm
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hawaii5oh
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Post by hawaii5oh on Apr 17, 2018 2:51:04 GMT -5
For Immediate Release April 14, 2018Vitakraft Sun Seed Recalls of Sunseed Vita Prima Sugar Glider Food Due to Possible Salmonella Health RiskVitakraft Sun Seed Inc. of Weston, OH, is voluntarily recalling one lot of Sunseed Vita Prima Exotics Sugar Glider Formula because it has the potential to be contaminated with Salmonella. Salmonella can affect animals eating the products and there is risk to humans from handling contaminated pet products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products. Healthy people infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers. Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever and abdominal pain. Infected but otherwise healthy pets can be carriers and infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian. Vitakraft Sun Seed was notified on April 13, 2018, by the Michigan Department of Agriculture that Salmonella was detected in an inspection sample of product from Lot Number 271391. The tests which discovered the bacteria were part of random testing regularly performed by the State of Michigan on various consumer products, and not prompted by any consumer concerns. To date there have been no reports of illness. Products matching the specific lot number below are being recalled: UPC # 87535-20060 DESCRIPTION Sunseed Vita Prima Exotics Sugar Glider Formula, 28oz LOT 271391 Exp: 12/20/19 “The health and happiness of our customers and their animal companions is always our top priority. We initiated our recall procedure as soon as we were notified of this issue so we could make sure pet owners were informed,” said Brent Weinmann, President & CEO of Vitakraft Sun Seed. The product was distributed to the following states: CA, FL, IL, MI, NJ, NV, OH, PA, and TX, as well as Edmonton, Alberta in Canada. Retailers and distributors who received the recalled lots have been contacted and asked to pull these lots from their inventory and shelves. Consumers who have purchased a product from the recalled lot should discontinue use of the product and may return the unused portion to the place of purchase for a full refund. Customers who have further questions are welcome to contact Customer Service at 1-800-221- 6175, Monday through Friday between 8:30am and 5:00pm EST. www.fda.gov/Safety/Recalls/ucm604674.htm
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hawaii5oh
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Post by hawaii5oh on Apr 17, 2018 2:53:48 GMT -5
For Immediate Release April 16, 2018Epic Products, LLC, Issues Voluntary Nationwide Recall of All Lots of Euphoric Capsules Due to Presence of Undeclared Sildenafil and TadalafilOverland Park, KS, Epic Products, LLC is voluntarily recalling all lots of Euphoric capsules, packaged in 1 count blister cards, 3 count bottles, and 12 count bottles to the consumer level. FDA analysis found samples of Euphoric to be tainted with undeclared sildenafil and tadalafil, active ingredients in two FDA-approved prescription drug products, also known as phosphodiesterase 5-inhibitors (PDE-5 inhibitors), used to treat male erectile dysfunction (ED). The presence of sildenafil and tadalafil in Euphoric renders it an unapproved drug for which safety and efficacy have not been established and, therefore subject to recall. Consumers who take this product for ED could have underlying cardiovascular disease. Consumers with diabetes, hypertension, high cholesterol or heart disease often take nitrates; concomitant use of nitrates and PDE-5 inhibitors can lead to fatal cardiovascular collapse. To date, Epic Products, LLC has not received any reports of adverse events related to this recall. This tainted Euphoric product is marketed as a dietary supplement for male sexual enhancement and is packaged in 1-count blister cards (UPC 6-9685928646-9), 3 count bottles (UPC 6-9685928646-6), and 12 count bottles (UPC 6-9685928648-3). All lots of Euphoric are included in this recall. Euphoric was sold to consumers nationwide in the USA via retail stores. Epic Products, LLC has discontinued sales of these products. Epic Products is notifying its distributors and customers by email and phone calls and is arranging for return of all recalled products. Consumers/Distributors/retailers that have Euphoric which is being recalled should stop use/distribution and return to place of purchase. Consumers with questions regarding this recall can call 1-800-589-1470 between the hours of 9:00am and 6:00pm CST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product. www.fda.gov/Safety/Recalls/ucm604729.htm
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hawaii5oh
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Post by hawaii5oh on Apr 17, 2018 2:59:06 GMT -5
Class I Recall 031-2018 Health Risk: High Apr 11, 2018 Conagra Brands Inc. Recalls Salisbury Steak Products Due to Possible Foreign Matter Contamination WASHINGTON, April 11, 2018 – Conagra Brands, Inc., a Russellville, Ark. establishment, is recalling approximately 135,159 pounds of Salisbury steak products (poultry, pork, and beef) that may be contaminated with extraneous materials, specifically bone, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The family-style, heat treated, not shelf stable Salisbury steak and brown gravy products were produced on March 10, 2018. The following products are subject to recall: label pictures27-oz. carton containing plastic shrink-wrapped packages containing 6 pieces of “Banquet FAMILY SIZE 6 SALISBURY STEAKS & BROWN GRAVY MADE WITH CHICKEN, PORK AND BEEF – GRILL MARKS ADDED” with lot code 5006 8069 10 05and a ‘BEST BY’ date of SEP 01 2019 printed on the package. The products subject to recall bear the USDA mark of inspection with establishment number “P-115” located on the side panel of the consumer package. These items were shipped to retail locations nationwide. The problem was discovered after the firm received several consumer complaints and three reports of minor oral injury associated with consumption of this product. Anyone concerned about an injury or illness should contact a healthcare provider. FSIS is concerned that some product may be frozen and in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2018/recall-031-2018-release
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hawaii5oh
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Post by hawaii5oh on Apr 17, 2018 3:04:31 GMT -5
Class II Recall 032-2018 Health Risk: Low Apr 11, 2018Koch Foods Inc. Recalls Beef Products Due to Possible Foreign Matter Contamination WASHINGTON, April 11, 2018 – Koch Foods, Inc., a Fairfield, Ohio establishment, is recalling approximately 119,480 pounds of beef rib-shaped patty products that may be contaminated with extraneous materials, specifically thin blue plastic pieces, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The fully cooked, not shelf stable rib-shaped beef patty with BBQ sauce products were produced on July 8, 2016. The following products are subject to recall: picture of the label (pdf)30-lb. bulk boxes containing 6 plastic shrink-wrapped unlabeled packages of “Fully Cooked Rib-Shaped Beef Patty With BBQ Sauce” and identified by case code “67329” and lot number “JTM 16190” represented on the label. The products subject to recall bear establishment number “EST. 20795” inside the USDA mark of inspection. These items were shipped to a distributors nationwide for institutional use. The problem was discovered when the firm received notification from a customer, and the firm notified FSIS on April 5, 2018. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider. FSIS is concerned that some product may be frozen and in consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. Consumers with questions about the recall can contact Mark Kaminsky, Quality Assurance Manager, at (847) 384-5940. Media with questions can contact James Bohlander, Recall Coordinator, at (513) 642-2653. www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2018/recall-032-2018-release
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hawaii5oh
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Post by hawaii5oh on Apr 17, 2018 3:09:20 GMT -5
Class I Recall 033-2018 Health Risk: High Apr 14, 2018 Fresh Foods Manufacturing Co. Recalls Ready-To-Eat Salad Products Due to Possible E. coli O157:H7 Contamination WASHINGTON, April 14, 2018 – Fresh Foods Manufacturing Co., a Freedom, Pa., establishment, is voluntarily recalling approximately 8,757 pounds of ready-to-eat salad products that may be contaminated with E. coli O157:H7, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The ready-to-eat salad products were produced from April 9, 2018 to April 12, 2018 and have a shelf life of four days. The following products are subject to recall: picture of the label (pdf) 11.5 oz., clear plastic containers of ready-to-eat “CAESAR SALAD WITH CHICKEN.” The product label is marked “Great to Go” by Market District and has a sell by date of 04/13/18-04/16/18. The case code is 81571201542. 14.4 oz., clear plastic containers of ready-to-eat “CHICKEN AND BACON” salad. The product label is marked “Great to Go” by Market District and has a sell by date of 04/13/18 – 04/16/18. The case code is 81571201541. • 14.1 oz., clear plastic containers of ready-to-eat “GARDEN SALAD WITH CHICKEN.” The product label is marked “Great to Go” by Market District and has a sell by date of 04/13/18 – 04/16/18. The case code is 81571201543. 13.1 oz., clear plastic containers of ready-to-eat “CHEF SALAD WITH HAM, TURKEY, & HARD-BOILED EGG.” The product label is marked “Great to Go” by Market District and has a sell by date of 04/13/18 – 04/16/18. The case code is 81571201545. The products subject to recall bear establishment number “P-40211” inside the USDA mark of inspection. These items were shipped to retail locations in Indiana, Ohio, Pennsylvania, and West Virginia. The problem was discovered on April 13, 2018 when Fresh Foods Manufacturing Co., received notification from their romaine lettuce supplier that the romaine lettuce used by the establishment in the products was being recalled due to E. coli O157:H7 concerns. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider. E. coli O157:H7 is a potentially deadly bacterium that can cause dehydration, bloody diarrhea and abdominal cramps 2–8 days (3–4 days, on average) after exposure the organism. While most people recover within a week, some develop a type of kidney failure called hemolytic uremic syndrome (HUS). This condition can occur among persons of any age but is most common in children under 5-years old and older adults. It is marked by easy bruising, pallor, and decreased urine output. Persons who experience these symptoms should seek emergency medical care immediately. Consumers and members of the media with questions about the recall can contact Dan Donovan, Director of Corporate Communications, Fresh Food Manufacturing Co. at (412) 967-4551. For additional information about the recall, customers may visit GiantEagle.com/Product-Recall. Customers may also contact Giant Eagle Customer Care via GiantEagle.com/contact or at 1-800-553-2324. Giant Eagle’s Customer Care service hours are Monday through Friday, from 9 a.m. to 9 p.m. EST. www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2018/recall-033-2018-release
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hawaii5oh
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Post by hawaii5oh on Apr 20, 2018 22:54:03 GMT -5
Posted April 20, 2018 4:00 PM ESTMultistate Outbreak of E. coli O157:H7 Infections Linked to Romaine LettuceHighlightsInformation collected to date indicates that romaine lettuce from the Yuma, Arizona growing region could be contaminated with E. coli O157:H7 and could make people sick. At this time, no common grower, supplier, distributor, or brand has been identified. What's New?Based on new information, CDC is expanding its warning to consumers to cover all types of romaine lettuce from the Yuma, Arizona growing region. This warning now includes whole heads and hearts of romaine lettuce, in addition to chopped romaine and salads and salad mixes containing romaine. Do not buy or eat romaine lettuce at a grocery store or restaurant unless you can confirm it is not from the Yuma, Arizona, growing region. Unless the source of the product is known, consumers anywhere in the United States who have any store-bought romaine lettuce at home should not eat it and should throw it away, even if some of it was eaten and no one has gotten sick. Product labels often do not identify growing regions; so, throw out any romaine lettuce if you’re uncertain about where it was grown. This includes whole heads and hearts of romaine, chopped romaine, and salads and salad mixes containing romaine lettuce. If you do not know if the lettuce is romaine, do not eat it and throw it away. Restaurants and retailers should not serve or sell any romaine lettuce from the Yuma, Arizona growing region. The expanded warning is based on information from newly reported illnesses in Alaska. Ill people in Alaska reported eating lettuce from whole heads of romaine lettuce from the Yuma, Arizona growing region. www.cdc.gov/ecoli/2018/o157h7-04-18/index.html
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hawaii5oh
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Post by hawaii5oh on Apr 20, 2018 23:53:23 GMT -5
Posted April 19, 2018 1:45 PM ETMultistate Outbreak of Salmonella Braenderup Infections Linked to Rose Acre Farms Shell EggsWhat's New?On April 16, 2018, Cal-Maine Foods, Inc. voluntarily recalled eggs purchased from Rose Acre Farms and produced at the Hyde County, North Carolina facility. Consumers, restaurants, and retailers should not eat, serve, or sell recalled eggs produced by Rose Acre Farms’ Hyde County farm. These eggs were sold under multiple brand names, including Coburn Farms, Country Daybreak, Food Lion, Glenview, Great Value, Nelms, Publix, Sunshine Farms, and Sunups. Check for eggs with plant number P-1065 and a Julian date between 011 and 102, or plant number P-1359D and Julian date 048A or 049A with Best By dates of APR 02 and APR 03. HighlightsConsumers, restaurants, and retailers should not eat, serve, or sell recalled eggs produced by Rose Acre Farms’ Hyde County farm. Throw them away or return them to the place of purchase for a refund. These eggs are sold under multiple brand names, including Coburn Farms, Country Daybreak, Food Lion, Glenview, Great Value, Nelms, Publix, Sunshine Farms, and Sunups. Check for eggs with plant number P-1065 and a Julian date between 011 and 102, or plant number P-1359D and Julian date 048A or 049A with Best By dates of APR 02 and APR 03. Visit the FDA website for a list of recalled products. Wash and sanitize drawers or shelves in refrigerators where recalled eggs were stored. Follow these five steps to clean your refrigerator. CDC, public health and regulatory officials in several states, and the U.S. Food and Drug Administration are investigating a multistate outbreak of Salmonella Braenderup infections linked to Rose Acre Farms shell eggs. Twenty-three people infected with the outbreak strain of Salmonella Braenderup have been reported from nine states. Six people have been hospitalized, and no deaths have been reported. Epidemiologic, laboratory, and traceback evidence indicates that shell eggs produced by Rose Acre Farms are the likely source of this multistate outbreak. www.cdc.gov/salmonella/braenderup-04-18/index.html
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hawaii5oh
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Post by hawaii5oh on Apr 22, 2018 23:48:25 GMT -5
For Immediate Release April 20, 2018OC Raw Dog, LLC RECALLS Freeze Dried Sardines BECAUSE PRODUCT EXCEEDS FDA SIZE RESTRICTIONSOC Raw Dog, LLC of Rancho Santa Margarita, CA, is recalling the Freeze Dried Sardines because the fish have exceeded the FDA compliance guideline for fish larger than 5 inches. The FDA has determined that salt-cured, dried, or fermented un-eviscerated fish larger than 5 inches have been linked to outbreaks of botulism poisoning between 1981 and 1987 and again in 1991. Because OC Raw Dog Freeze Dried Sardines are larger than 5 inches there is a possible health risk. Clostridium botulinum can cause severe and potentially fatal toxicity in both animals consuming the pet treat and people handling the pet treat or coming in contact with contact areas that have been exposed o the product. Common symptoms may include dizziness, blurred or double vision, trouble with speaking or swallowing, difficulty breathing, muscle weakness, abdominal distension, and constipation. Pets or Persons experiencing these symptoms should seek immediate medical attention. This product of Freeze Dried Sardines was shipped to Distributors in the following states with the intent to be sold to Wholesales who in turn sell to Consumers. This product would be found in Independent Pet Specialty Stores within the following states:
California, Colorado, Florida, Maryland, Minnesota, Texas, and Pennsylvania.
OC Raw Dog Freeze Dried Sardines are packaged in a 3.2 oz bag with a UPC of 095225853043.To date there have been no reported illnesses of dogs, cats, or persons in any connection with the sardines. OC Raw was notified by the Minnesota Department of Food and Agriculture after a sample of our OC Raw Dog Freeze Dried Sardines were collected and determined to contain un-eviscerated or intact un-gutted fish that measure 6-61/2 inches which is greater than FDA guidelines of 5 inches for un-eviscerated fish. This product has not tested positive for Clostridium botulinum. Minnesota Department of Food and Agriculture tested the product for Salmonella where the test returned negative. Distributors, Retailers and Consumers who have purchased OC Raw Dog’s Freeze Dried Sardines can return it to the location where it was purchased for a full refund. Consumers with questions may contact the company at 1-844-215-DOGS Monday – Friday 8am – 5pm PST www.fda.gov/Safety/Recalls/ucm605370.htm
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hawaii5oh
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Post by hawaii5oh on Apr 22, 2018 23:51:14 GMT -5
For Immediate Release April 20, 2018OC Raw Dog, LLC RECALLS one lot of Chicken, Fish & Produce BECAUSE OF POSSIBLE HEALTH RISKOC Raw Dog, LLC of Rancho Santa Margarita, CA, is recalling approximately 1,560 lbs of Chicken, Fish & Produce Raw Frozen Canine Formulation which was manufactured on 10/11/2017 with a lot number 3652 and a use by date of 10/11/18. We are voluntarily recalling because of potential contamination with Listeria monocytogenes, which can cause severe and potentially fatal infection in animals consuming the pet food, and the humans that handle the pet food and surfaces exposed to the product. Pets can be carriers of the bacteria and infect humans, even if the pets do not appear to be ill. Short-term symptoms may include high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea. Young children, frail or elderly people, and others with weakened immune systems are particularly vulnerable to Listeria monocytogenes infections, which can cause miscarriages and stillbirths among pregnant women. Healthy people infected with Listeria monocytogenes should monitor themselves and their pets for symptoms. Lot # 3652 of OC Raw Dog Chicken, Fish & Produce was shipped to the following states with the following associated volume with the intent to sell to Independent Specialty Retailers and in turn sold to Consumers. California – 356 lbs., Colorado – 153 lbs., Florida – 195 lbs., Maryland – 320 lbs., Minnesota – 429 lbs., Pennsylvania – 78 lbs. and Vermont – 30 lbs. This lot of OC Raw Dog Chicken, Fish & Produce was made into 3 lb. Meaty Rox Bags, 4 lb. Slider Bags, 6.5 lb. Doggie Dozen Patty Bags and 7 lb. Meaty Rox Bags. All of which have been marked with a lot number of 3652 and a USE BY DATE of 10/11/18. Each bag has this information on a sticker located on the back lower left corner of the bag.
[click on the link below to view the UPC barcodes] To date there have been no reported illnesses of dogs, cats or persons in any connection with this product. The contamination is still under investigation. OC Raw was notified by the FDA of the contamination after it was reported that New Jersey Department of Food and Agriculture tested the product and found it to be positive. The same lab who conducted the tests for Listeria also tested for Salmonella on our 3 lb. bag of Chicken, Fish & Produce Meaty Rox and the test was negative. In addition to the OC Raw Dog Chicken, Fish & Produce tests the lab conducted tests for OC Raw Dog Pumpkin Rox for Listeria monocytogenes and Salmonella and the results were negative. There was product at two of the seven distribution locations. The product has been pulled from inventory and destroyed. It is possible there might be a few bags at retailers or at home with consumers. We strongly urge anyone who has purchased OC Raw Dog’s Chicken, Fish & Produce to check the lot number. Consumers who have purchased product with lot 3652 are urged to return it to the Retailer where it was purchase for a full refund. Consumers with questions may contact the company at 1-844-215-DOGS Monday – Friday 8am – 5pm PST. www.fda.gov/Safety/Recalls/ucm605374.htm
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hawaii5oh
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Post by hawaii5oh on Apr 22, 2018 23:53:47 GMT -5
For Immediate Release April 21, 2018Voluntary Recall Notice of Happy Harvest Canned Spinach Due to Potential Undeclared Peanut Allergen from Product MislabelingMcCall Farms, Inc. is voluntarily recalling a limited amount of cases of Happy Harvest Spinach in 13.5 oz cans as a precautionary measure due to the potential presence of peanuts resulting from product mislabeling. This product may cause an allergic reaction in customers who have a peanut allergy. In cooperation with ALDI, all affected product has been removed from its stores. ALDI is the only retailer with this product. The product was packaged in 13.5 oz cans with the lot code of A23IX. The best-by date is January 2021. The UPC code is 041498131289.
The product was available for purchase in the following states: Florida, Georgia, Iowa, Illinois, Indiana, Kentucky, Michigan, Minnesota, North Carolina, Ohio, South Carolina, South Dakota, Tennessee, Virginia, Wisconsin, and West Virginia.
The product was also available for purchase to ALDI customers in the Atlanta and Chicago areas through the company's partnership with Instacart, a grocery delivery service.To date, no illnesses related to this product have been reported. No other ALDI or McCall Farms products are affected by this recall. McCall Farms takes the safety and integrity of all its products very seriously. If consumers have product affected by this voluntary recall, they should discard it immediately or return it to the local ALDI store for a full refund. Customers who have questions may contact McCall Farms consumer services at customerservice@mccallfarms.com or 1-800-277-2012. www.fda.gov/Safety/Recalls/ucm605388.htm
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hawaii5oh
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Post by hawaii5oh on Apr 25, 2018 6:17:00 GMT -5
For Immediate Release April 23, 2018Nutrizone Expands Recalls of Various Lots of Multiple Dietary Supplements to Include All Kratom Products and All Lots Because of Possible Salmonella Health RiskNutriZone, LLC of Houston, Texas is expanding its recall of various kratom dietary supplements to all lots sold, which may contain the same source material as the original recalled lots. The expanded recall is being conducted out of an abundance of caution. The recall of dietary supplements is due to the potential for contamination with Salmonella. Salmonella, is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy people infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers. The dietary supplements are labeled and packaged as follows: [click on the link below to view the recalled products]The products were sold Nationwide (FL, CA, OK, GA, SC, PA, LA, WA, MS, MO, KY, AZ, CO, TX, NY, IL). No illnesses have been reported to date in connection with this problem. The potential for contamination was noted after routine sampling and testing by the FDA revealed the presence of Salmonella. Consumers who have purchased the products listed above should discontinue use of the product and may return the unused portion to the place of purchase for a full refund. Consumers with questions may contact NutriZone, LLC, at 1-800-936-7936, Monday through Friday, 9am-5pm Central Standard time. www.fda.gov/Safety/Recalls/ucm603356.htm
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