FDA Classifies Q’Apel Medical Inc.’s Worldwide Medical Device Recall and Discontinuation of its 072 Aspiration System (Hippo) as Class I

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On April 7, 2025, the U.S. Food and Drug Administration (“FDA” or “the agency”), classified Q’Apel Medical, Inc.’s (“Q’Apel” or “the company”) voluntary recall of 1,617 units of its 072 Aspiration System (also known under the product name “Hippo”, which includes “Cheetah”; collectively, the “product

Source: Food and Drugs Administration--Recalls/Safety Alerts

FDA Classifies Q’Apel Medical Inc.’s Worldwide Medical Device Recall and Discontinuation of its 072 Aspiration System (Hippo) as Class I

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On April 7, 2025, the U.S. Food and Drug Administration (“FDA” or “the agency”), classified Q’Apel Medical, Inc.’s (“Q’Apel” or “the company”) voluntary recall of 1,617 units of its 072 Aspiration System (also known under the product name “Hippo”, which includes “Cheetah”; collectively, the “product

Source: Food and Drugs Administration--Recalls/Safety Alerts

Amneal Pharmaceutical LLC Issues a Nationwide Recall of Ropivacaine Hydrochloride Injection, USP 500mg/100mL, Due to the Potential Presence of Particulate Matter

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Bridgewater, NJ, Amneal Pharmaceutical LLC, is recalling two lots of Ropivacaine Hydrochloride Injection, USP, 500mg/100mL, Infusion bags to the hospital/user level as the products may contain an inert fiber identified as polypropylene fibers from the IV bag.

Source: Food and Drugs Administration--Recalls/Safety Alerts

Amneal Pharmaceutical LLC Issues a Nationwide Recall of Ropivacaine Hydrochloride Injection, USP 500mg/100mL, Due to the Potential Presence of Particulate Matter

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Bridgewater, NJ, Amneal Pharmaceutical LLC, is recalling two lots of Ropivacaine Hydrochloride Injection, USP, 500mg/100mL, Infusion bags to the hospital/user level as the products may contain an inert fiber identified as polypropylene fibers from the IV bag.

Source: Food and Drugs Administration--Recalls/Safety Alerts

Recall Reminder: Gerber Products Company Previously Recalled and Discontinued All Batches of Gerber® Soothe N Chew® Teething Sticks Due To Potential Choking Hazard

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On January 31, 2025, Gerber Products Company initiated a recall and discontinuation of all batches of GERBER® SOOTHE N CHEW® TEETHING STICKS due to a potential choking hazard for babies and young children.

Source: FDA Food Safety Recalls RSS Feed

Harvest NYC Inc Recalls Enoki Mushroom Due to Possible Health Risk

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Harvest NYC Inc of Brooklyn, NY 11231 is recalling its 200g packages of Enoki Mushroom, because they may be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems.

Source: FDA Food Safety Recalls RSS Feed

Supplement Manufacturing Partner, Inc. Issues Recall on Dorado Nutrition Brand Spermidine Supplement 10mg Vegetable Capsules (Spermidine 3HCL) Due To Undeclared Wheat Allergen

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Supplement Manufacturing Partners, Inc. is recalling Dorado Nutrition brand Spermidine Maximum Strength 10 MG per serving, because it contains undeclared wheat. People who have an allergy or severe sensitivity to wheat run the risk of serious or life-threatening allergic reaction if they consume thi

Source: Food and Drugs Administration--Recalls/Safety Alerts

May Flower International Inc., Issue Allergy Alert on Undeclared Wheat in “Beijing Soybean Paste”

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May Flower International Inc of Maspeth, NY, is recalling its 8.82-ounce/250g packages of “Beijing Soybean Paste” food treats because they may contain undeclared wheat. People who have allergies to wheat run the risk of serious or life-threatening allergic reaction if they consume these products.

Source: Food and Drugs Administration--Recalls/Safety Alerts

Blue Ridge Beef Issues Voluntary Recall of Blue Ridge Beef Puppy Mix and Kitten Mix Due to Salmonella & Listeria Contamination

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Blue Ridge Beef is recalling 1,080 lbs. of their 2 lb logs of Kitten Mix Lot # N26 0114 and 1,380 lbs of their 2 lb logs of Puppy Mix Lot # N25 1230 (Lot numbers are stamped in the clips on the end of the chubs/bags) due to contamination with Salmonella and Listeria.

Source: Food and Drugs Administration--Recalls/Safety Alerts

Duda Farm Fresh Foods, Inc. Emite Aviso Para 1.587 Cajas de Marketside 4in/1.6 oz Bundle Pack por Posible Riesgo Para la Salud Celery Sticks

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Duda Farm Fresh Foods, Inc. emite voluntariamente una advertencia preventiva sobre un lote de producción de palitos de apio Marketside de 4 pulgadas/1.6 oz, lavados y listos para consumir, con fecha de caducidad del 23/03/2025.

Source: FDA Food Safety Recalls RSS Feed