My Life Inc Issues Allergy Alert on Undeclared Milk in ML Natural Premium Quality Lactoferrin as Apolactoferrin

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April 25, 2025, My Life Inc. of Federal Way, WA is recalling approximately 65 bottles of ML Naturals Premium Quality Lactoferrin as Apolactoferrin 300mg. capsules dietary supplement, lot FL2407511L19, expiration date 10/2027, because it may contain undeclared milk. People who have an allergy or seve

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

New England Village Foods Issues Allergy Alert on Undeclared Almonds in “19th Hole Snack Mix”

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New England Village Foods of Milford NH is recalling all lots of 5 -ounce and 10 -ounce containers of New England Village Snacks “19th Hole Snack Mix” because they may contain undeclared almonds. People who have allergies to almonds run the risk of serious or life-threatening allergic reaction if th

Source: FDA Food Safety Recalls RSS Feed

Cronus Pharma LLC initiating Voluntary Recall for (Dexased™ -Aspen and Dexmedvet™ -Cronus Pharma LLC) of Dexmedetomidine Hydrochloride Injection 0.5 mg/mL For Veterinary Use Due to Presence of Particulate Matter

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East Brunswick, NJ, April 23, 2025 - CRONUS PHARMA LLC, on behalf of Cronus Pharma Specialities, Hyderabad, India is issuing a voluntary recall involving one batch comprising two distinct lots: Dexased™ (Aspen) and Dexmedvet™ (Cronus Pharma LLC). Both products contain Dexmedetomidine Hydrochloride I

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

Cronus Pharma LLC initiating Voluntary Recall for (Dexased™ -Aspen and Dexmedvet™ -Cronus Pharma LLC) of Dexmedetomidine Hydrochloride Injection 0.5 mg/mL For Veterinary Use Due to Presence of Particulate Matter

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East Brunswick, NJ, April 23, 2025 - CRONUS PHARMA LLC, on behalf of Cronus Pharma Specialities, Hyderabad, India is issuing a voluntary recall involving one batch comprising two distinct lots: Dexased™ (Aspen) and Dexmedvet™ (Cronus Pharma LLC). Both products contain Dexmedetomidine Hydrochloride I

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

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