Food and Drugs Administration--Recalls/Safety Alerts http://www.fda.gov/ en Merck Animal Health Expands Voluntary Recall with Four Additional Lots of BANAMINE® / BANAMINE®-S (flunixin meglumine injection) in the U.S., Due to Presence of Particulate Matter http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/merck-animal-health-expands-voluntary-recall-four-additional-lots-banaminer-banaminer-s-flunixin Merck Animal Health, known as MSD Animal Health outside of the United States and Canada, a division of Merck &amp; Co., Inc., Rahway, N.J., USA (NYSE:MRK), is voluntarily recalling four additional batches of BANAMINE® / BANAMINE®-S (flunixin meglumine injection) 50 mg/mL in the United States, used for i Fri, 29 Sep 2023 00:00:00 EDT FDA http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/merck-animal-health-expands-voluntary-recall-four-additional-lots-banaminer-banaminer-s-flunixin Dick Taylor Craft Chocolate Issues Recall for Allergy Allert on Undeclared Peanuts in “Ginger Snap Milk Chocolate” http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/dick-taylor-craft-chocolate-issues-recall-allergy-allert-undeclared-peanuts-ginger-snap-milk Dick Taylor Craft Chocolate of Eureka, California is recalling “Ginger Snap Milk Chocolate” batch 23194 because they were mis-packaged and are Peanut Butter Dark Chocolate bars in Ginger Snap wrappers and contain undeclared peanuts. People who have allergies to peanuts are at risk of serious life-th Thu, 28 Sep 2023 00:00:00 EDT FDA http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/dick-taylor-craft-chocolate-issues-recall-allergy-allert-undeclared-peanuts-ginger-snap-milk Penzeys Spices Issues Allergy Alert on Undeclared Sesame Seeds in "Brady Street Cheese Sprinkle" http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/penzeys-spices-issues-allergy-alert-undeclared-sesame-seeds-brady-street-cheese-sprinkle Penzeys Spices of Wauwatosa, WI, is voluntarily recalling some of its 2.2-ounce Jars of Brady Street Cheese Sprinkle (SKU/Item Number 20756) because they may contain undeclared sesame seeds. People who have allergies to sesame seeds run the risk of serious or life-threatening allergic reactions if t Thu, 28 Sep 2023 00:00:00 EDT FDA http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/penzeys-spices-issues-allergy-alert-undeclared-sesame-seeds-brady-street-cheese-sprinkle Eagle Produce LLC Recalls Whole Cantaloupe Because of Possible Health Risk http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/eagle-produce-llc-recalls-whole-cantaloupe-because-possible-health-risk Eagle Produce LLC Scottsdale, AZ is initiating a voluntary recall of 6,456 cases of whole cantaloupe with the potential to be contaminated with Salmonella following a test conducted on cantaloupe in a distribution center by the FDA. Salmonella is an organism which can cause serious and sometimes fat Wed, 27 Sep 2023 00:00:00 EDT FDA http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/eagle-produce-llc-recalls-whole-cantaloupe-because-possible-health-risk SCYNEXIS Issues a Voluntary Nationwide Recall of BREXAFEMME® (ibrexafungerp tablets) Due to Potential for Cross Contamination with a Non-Antibacterial ßlactam Drug Substance http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/scynexis-issues-voluntary-nationwide-recall-brexafemmer-ibrexafungerp-tablets-due-potential-cross SCYNEXIS, Inc. is conducting a voluntary nationwide recall of 2 lots of BREXAFEMME® (ibrexafungerp tablets) to the consumer level in the US market due to potential cross contamination with a nonantibacterial<br /> ß-lactam drug substance in the ibrexafungerp citrate used to manufacture the BREXAFEMME® tab Wed, 27 Sep 2023 00:00:00 EDT FDA http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/scynexis-issues-voluntary-nationwide-recall-brexafemmer-ibrexafungerp-tablets-due-potential-cross Safeway Fresh Foods Recalls Sunnyside Farms Organic Butternut Squash Because of Possible Health Risk http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/safeway-fresh-foods-recalls-sunnyside-farms-organic-butternut-squash-because-possible-health-risk Safeway Fresh Foods of Vineland, NJ, is recalling its 32-oz. Diced Organic Butternut Squash product as it has the potential to be contaminated with Escherichia coli O45. E. coli O45 causes a diarrheal illness often with bloody stools. Although most healthy adults can recover completely within a week Mon, 25 Sep 2023 00:00:00 EDT FDA http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/safeway-fresh-foods-recalls-sunnyside-farms-organic-butternut-squash-because-possible-health-risk VistaPharm LLC Issues Voluntary Nationwide Recall of Sucralfate Oral Suspension, 1g/10mL Due to Microbial Contamination Identified as Bacillus Cereus http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/vistapharm-llc-issues-voluntary-nationwide-recall-sucralfate-oral-suspension-1g10ml-due-microbial September 22, 2023 – Largo, Florida, VistaPharm LLC is voluntarily recalling one (1) lot of Sucralfate Oral Suspension, 1g/10mL, to the consumer level, due to Bacillus cereus contamination in the product. Fri, 22 Sep 2023 18:31:00 EDT FDA http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/vistapharm-llc-issues-voluntary-nationwide-recall-sucralfate-oral-suspension-1g10ml-due-microbial TAMA Corporation Emite Un Alerta De Alergenos No Declarados: Trigo, Soya y Amarillo #5 En Las “Cachapas De Maiz Paisa” http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/tama-corporation-emite-un-alerta-de-alergenos-no-declarados-trigo-soya-y-amarillo-5-en-las-cachapas Tama Corp. de Doral, FL, alerta que su producto &quot;Cachapas de Maiz Paisa&quot;, en paquetes de 24 oz, contiene alergenos no declarados en la etiqueta: Trigo, Soya y Amarillo #5. Personas alérgicas a estos ingredientes corren el riesgo de reacciones alérgicas serias e incluso graves si consumen el producto Fri, 22 Sep 2023 00:00:00 EDT FDA http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/tama-corporation-emite-un-alerta-de-alergenos-no-declarados-trigo-soya-y-amarillo-5-en-las-cachapas TAMA Corporation Issues Allergy Alert for Undeclared Wheat, Soy and Yellow #5 in "Cachapas de Maiz PAISA" http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/tama-corporation-issues-allergy-alert-undeclared-wheat-soy-and-yellow-5-cachapas-de-maiz-paisa Tama Corp. of Doral, FL, is recalling its 24-ounce packages of &quot;Cachapas de Maiz Paisa&quot; because they contain undeclared wheat, soy and Yellow #5. People who have allergies to any of these run the risk of serious or life-threatening allergic reaction if they consume these products. Thu, 21 Sep 2023 00:00:00 EDT FDA http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/tama-corporation-issues-allergy-alert-undeclared-wheat-soy-and-yellow-5-cachapas-de-maiz-paisa Life Raft Treats has Expanded their Recalls of Ice Cream Products, Not Fried Chicken And Life Is Peachy, Due to Possible Listeria Monocytogenes Contamination http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/life-raft-treats-has-expanded-their-recalls-ice-cream-products-not-fried-chicken-and-life-peachy-due Life Raft Treats is expanding their recall of their Not Fried Chicken 64 oz bucket, Not Fried Chicken 2.5 oz bar UPC 8 60006 18210 6 and Life Is Peachy 6 count box ice cream products, to include the BEST BY DATES up<br /> to and including AUG 08282024 due to a potential contamination of Listeria monocytog Tue, 19 Sep 2023 00:00:00 EDT FDA http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/life-raft-treats-has-expanded-their-recalls-ice-cream-products-not-fried-chicken-and-life-peachy-due Kraft Heinz Issues Voluntary Recall of Select Kraft Singles American Processed Cheese Slices http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/kraft-heinz-issues-voluntary-recall-select-kraft-singles-american-processed-cheese-slices Kraft Heinz is announcing a voluntary recall of approximately 83,800 cases of individually-wrapped Kraft Singles American processed cheese slices that were shipped to a limited number of customers. The voluntary recall comes as a precaution after a temporary issue developed on one of our wrapping ma Tue, 19 Sep 2023 00:00:00 EDT FDA http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/kraft-heinz-issues-voluntary-recall-select-kraft-singles-american-processed-cheese-slices Allergen Alert on Undeclared Peanuts in "Cake" http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/allergen-alert-undeclared-peanuts-cake David’s Cookies is recalling 960 units of “Marketside Chocolate Chip Explosion Cake” lot # BS23212 that has been sold in Walmart retail stores across the country. This recall is due to that the 960 units of “Marketside Ultimate Peanut Butter Chocolate Cake” ware mislabeled with a label as “Marketsid Tue, 19 Sep 2023 00:00:00 EDT FDA http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/allergen-alert-undeclared-peanuts-cake Knickerbocker 365 Issues Allergy Alert on Undeclared Milk in “Homestyle Hamburger Buns” http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/knickerbocker-365-issues-allergy-alert-undeclared-milk-homestyle-hamburger-buns Knickerbocker 365, Inc. of Madison Heights, MI, is recalling its 16-ounce packages of &quot;Homestyle Hamburger Buns&quot; because they contain undeclared milk. Thu, 14 Sep 2023 18:00:00 EDT FDA http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/knickerbocker-365-issues-allergy-alert-undeclared-milk-homestyle-hamburger-buns Church & Dwight Issues Voluntary Nationwide Recall of One Specific Lot of TheraBreath Strawberry Splash for Kids 16oz Sold Exclusively on Amazon Between May 31 and September 02, 2023, Due to Microbial Contamination Identified as Yeast (Candida Parapsilosis) http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/church-dwight-issues-voluntary-nationwide-recall-one-specific-lot-therabreath-strawberry-splash-kids FOR IMMEDIATE RELEASE – September 13, 2023 – EWING, N.J – Church &amp; Dwight Co., Inc. (NYSE:CHD) today initiated a voluntary recall of one specific lot of TheraBreath Strawberry Splash for Kids 16oz after the Company identified a microbial contamination due to the presence of yeast (Candida Parapsilo Wed, 13 Sep 2023 00:00:00 EDT FDA http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/church-dwight-issues-voluntary-nationwide-recall-one-specific-lot-therabreath-strawberry-splash-kids Universal Meditech Inc. Expands Nationwide Recall to All Products Manufactured between March 2021 and November 2022 http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/universal-meditech-inc-expands-nationwide-recall-all-products-manufactured-between-march-2021-and Universal Meditech Inc. initiated a nationwide recall of products it manufactured between March 2021 and November 2022. The recall is due to the reasons that: i. The company is going out of business, hence would not be able to continue fulfilling any post-market responsibilities of these distributed Wed, 13 Sep 2023 00:00:00 EDT FDA http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/universal-meditech-inc-expands-nationwide-recall-all-products-manufactured-between-march-2021-and Sheng Kee of California, Inc. Issues Allergy Alert on Undeclared Egg in the Following Traditional Mooncake Products http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sheng-kee-california-inc-issues-allergy-alert-undeclared-egg-following-traditional-mooncake-products Sheng Kee of California, Inc. is voluntarily recalling varieties of Mooncake Gift Boxes for customers that have any issues because they may contain undeclared egg wash. People who have allergies to egg run the risk of serious or life-threatening allergic reaction if they consume these products. Mon, 11 Sep 2023 15:41:00 EDT FDA http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sheng-kee-california-inc-issues-allergy-alert-undeclared-egg-following-traditional-mooncake-products Novartis Issues Voluntary Nationwide Recall of One Lot of Sandimmune® Oral Solution (Cyclosporine Oral Solution, USP), 100 mg/mL Due to Crystallization http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/novartis-issues-voluntary-nationwide-recall-one-lot-sandimmuner-oral-solution-cyclosporine-oral Novartis is conducting a voluntary nationwide recall at the consumer level of one lot of its Sandimmune® Oral Solution (cyclosporine oral solution, USP), 100 mg/mL in the US due to crystal formation observed in some bottles, which could potentially result in incorrect dosing. No other Sandimmune for Mon, 11 Sep 2023 13:11:00 EDT FDA http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/novartis-issues-voluntary-nationwide-recall-one-lot-sandimmuner-oral-solution-cyclosporine-oral OBC Group Corp Retira Del Mercado Productos De Semillas Y Cápsulas De Nuez De La India Debido A Posibles Riesgos Para La Salud http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/obc-group-corp-retira-del-mercado-productos-de-semillas-y-capsulas-de-nuez-de-la-india-debido OBC GROUP CORP de, Miami, FL está retirando del mercado sus semillas y capsulas NUT DIET MAX Nuez de la India porque un análisis de la FDA ha determinado que los productos parecen ser Thevetia peruviana o adelfa amarilla. Se sabe que todas las partes de la planta de adelfa amarilla contienen glucósi Wed, 06 Sep 2023 14:09:00 EDT FDA http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/obc-group-corp-retira-del-mercado-productos-de-semillas-y-capsulas-de-nuez-de-la-india-debido OBC Group Corp Recalls Nuez de la India Seeds and Capsules Products Due to Possible Health Risks http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/obc-group-corp-recalls-nuez-de-la-india-seeds-and-capsules-products-due-possible-health-risks OBC GROUP CORP of, Miami, FL is recalling its NUT DIET MAX Nuez de la India Seeds and Capsules because FDA analysis has determined that the products appear to be Thevetia peruviana, or yellow oleander. All parts of the yellow oleander plant are known to contain cardiac glycosides that are highly tox Wed, 06 Sep 2023 13:58:00 EDT FDA http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/obc-group-corp-recalls-nuez-de-la-india-seeds-and-capsules-products-due-possible-health-risks Life Raft Treats Recalls Ice Cream Products, Not Fried Chicken And Life Is Peachy, Due to Possible Listeria Monocytogenes Contamination http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/life-raft-treats-recalls-ice-cream-products-not-fried-chicken-and-life-peachy-due-possible-listeria Life Raft Treats is recalling their Not Fried Chicken 64 oz bucket, Not Fried Chicken 2.5 oz bar UPC 8 60006 18210 6 and Life Is Peachy 6 count box ice cream products, all with BEST BY DATES up to and including AUG 8212024 due to a potential contamination of Listeria monocytogenes. Listeria monoc Wed, 06 Sep 2023 00:00:00 EDT FDA http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/life-raft-treats-recalls-ice-cream-products-not-fried-chicken-and-life-peachy-due-possible-listeria