Product Recalls in Mississippi
Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,423 recalls have been distributed to Mississippi in the last 12 months.
Showing 37521–37540 of 49,744 recalls
Recalled Item: 3.2 mm Cannulated Drill Bit/ QC 170 mm 2.7 Cannulated Recalled by Synthes,...
The Issue: affected parts and lots of the Cannulated Drill Bits have the potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fentanyl Citrate Inj. Recalled by West-Ward Pharmaceutical Corp. Due to...
The Issue: Failed Impurities/Degradation Specifications; 12 month stability testing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Outer carton : Nabisco Newtons Fig 24-2 OZ (56 g) Recalled by Mondelez...
The Issue: Fig Newtons brand Club Super Carton cookie products is mislabeled. The outer...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Optilite Analyser Recalled by The Binding Site Group, Ltd. Due to Potential...
The Issue: Potential risk of the Optilite lid/cover falling suddenly and causing injury...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Famotidine Tablets Recalled by Allegiant Health Due to CGMP Deviations:...
The Issue: CGMP Deviations: Failure of the manufacturer, Wockhardt Ltd, to adequately...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: T.A.L.O.N (Tactically Advanced Lifesaving Intraosseous Needle) 15G x 38.5 mm...
The Issue: Potential breach in sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ReUnion TSA Shoulder System Recalled by Stryker Howmedica Osteonics Corp....
The Issue: A package labeled as Part #5901-S-4818, Lot MAC7C14, standard humeral head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVOTECH Endoscope Cleaner and Reprocessing System 220-230V Recalled by...
The Issue: Advanced Sterilization Products (ASP) is recalling the EVOTECH Endoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alkaline Wash Recalled by Abbott Laboratories Due to The product is leaking...
The Issue: The product is leaking from the cap and crystallization was noted as present...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVOTECH Endoscope Cleaner and Reprocessing System 208V Recalled by Advanced...
The Issue: Advanced Sterilization Products (ASP) is recalling the EVOTECH Endoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Centurion POCT System Drill Guide PN 69-1010 and PN Recalled by...
The Issue: There is a possibility that the thumb button remains in the depressed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zebeta¿ (bisoprolol fumarate) Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Failed Dissolution Specifications: OOS result during stability testing
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Shiley Neonatal Recalled by Covidien LP (formerly Nellcor Puritan Bennett...
The Issue: Reports where patients who recently switched from the current Shiley...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RaySearch RayStation 2.5 Recalled by RAYSEARCH LABORATORIES AB Due to...
The Issue: RaySearch Laboratories AB became aware of an issue with the dose calculation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ethicon Fast Absorbing Plain Gut - MultiPass Needles Recalled by Ethicon,...
The Issue: Ethicon Fast Absorbing Surgical Gut (Plain) Suture is being recalled because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0210-312-000-Woundcare Replacement kit with soft tip Recalled by Stryker...
The Issue: Potential sterility breach in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gyrus ACMI Diego Elite Tubeset Recalled by Gyrus Acmi, Incorporated Due to...
The Issue: Potential lack of sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shiley Neonatal Recalled by Covidien LP (formerly Nellcor Puritan Bennett...
The Issue: Reports where patients who recently switched from the current Shiley...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gyrus ACMI Diego Elite Tubeset Recalled by Gyrus Acmi, Incorporated Due to...
The Issue: Potential lack of sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 250cc White Plastic Container containing 120 capsules Recalled by Natural...
The Issue: Natural Creations announces allergy alert and voluntary recall of New...
Recommended Action: Do not consume. Return to store for a refund or discard.