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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 FDA
  • April 23, 2025

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

East Brunswick, NJ, April 23, 2025 – CRONUS PHARMA LLC, on behalf of Cronus Pharma Specialities, Hyderabad, India is issuing…
fda-classifies-q’apel-medical-inc.’s-worldwide-medical-device-recall-and-discontinuation-of-its-072-aspiration-system-(hippo)-as-class-i FDA
  • April 19, 2025

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

On April 7, 2025, the U.S. Food and Drug Administration (“FDA” or “the agency”), classified Q’Apel Medical, Inc.’s (“Q’Apel” or…
amneal-pharmaceutical-llc-issues-a-nationwide-recall-of-ropivacaine-hydrochloride-injection,-usp-500mg/100ml,-due-to-the-potential-presence-of-particulate-matter FDA
  • April 18, 2025

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

Bridgewater, NJ, Amneal Pharmaceutical LLC, is recalling two lots of Ropivacaine Hydrochloride Injection, USP, 500mg/100mL, Infusion bags to the hospital/user…
early-alert:-intravascular-picc-catheter-issue-from-bd FDA
  • April 18, 2025

Early Alert: Intravascular PICC Catheter Issue from BD

This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
recall-reminder:-gerber-products-company-previously-recalled-and-discontinued-all-batches-of-gerber-soothe-n-chew-teething-sticks-due-to-potential-choking-hazard FDA
  • April 18, 2025

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

On January 31, 2025, Gerber Products Company initiated a recall and discontinuation of all batches of GERBER® SOOTHE N CHEW®…
early-alert:-diagnostic-intravascular-catheter-issue-from-conavi FDA
  • April 18, 2025

Early Alert: Diagnostic Intravascular Catheter Issue from Conavi

This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
harvest-nyc-inc-recalls-enoki-mushroom-due-to-possible-health-risk FDA
  • April 16, 2025

Harvest NYC Inc Recalls Enoki Mushroom Due to Possible Health Risk

Harvest NYC Inc of Brooklyn, NY 11231 is recalling its 200g packages of Enoki Mushroom, because they may be contaminated…
supplement-manufacturing-partner,-inc.-issues-recall-on-dorado-nutrition-brand-spermidine-supplement-10mg-vegetable-capsules-(spermidine-3hcl)-due-to-undeclared-wheat-allergen FDA
  • April 14, 2025

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

Supplement Manufacturing Partners, Inc. is recalling Dorado Nutrition brand Spermidine Maximum Strength 10 MG per serving, because it contains undeclared…
may-flower-international-inc.,-issue-allergy-alert-on-undeclared-wheat-in-“beijing-soybean-paste” FDA
  • April 11, 2025

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

May Flower International Inc of Maspeth, NY, is recalling its 8.82-ounce/250g packages of “Beijing Soybean Paste” food treats because they…
blue-ridge-beef-issues-voluntary-recall-of-blue-ridge-beef-puppy-mix-and-kitten-mix-due-to-salmonella-&-listeria-contamination FDA
  • April 11, 2025

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

Blue Ridge Beef is recalling 1,080 lbs. of their 2 lb logs of Kitten Mix Lot # N26 0114 and…