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. 2,465 recalls have been distributed to Mississippi in the last 12 months.
Showing 24121–24140 of 49,744 recalls
Recalled Item: AVS Aria Cage Recalled by Stryker Spine Due to The anterior and posterior...
The Issue: The anterior and posterior markers on the cage were on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK(R) 2 AST-P655 Recalled by bioMerieux, Inc. Due to Routine internal...
The Issue: Routine internal review of Device History Records identified six VITEK(R) 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK(R) 2 AST-P640 Recalled by bioMerieux, Inc. Due to Routine internal...
The Issue: Routine internal review of Device History Records identified six VITEK(R) 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IsoFlex LAL Support Surface Recalled by Stryker Medical Division of Stryker...
The Issue: Certain 2860 IsoFlex LAL support surfaces were assembled with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VaccZyme Human Anti-Haemophilus influenza type b Enzyme Immunoassay Kit For...
The Issue: A deterioration of performance was identified with influenza type B Enzyme...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cyclosporine 1% Human Eye Drops Recalled by Westlab Pharmacy, Inc. dba...
The Issue: Lack of Process Controls
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ADAA Cataract Drops Recalled by Westlab Pharmacy, Inc. dba Westlab Pharmacy...
The Issue: Lack of Process Controls
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprostadil 500 mcg/mL Injectable Recalled by Westlab Pharmacy, Inc. dba...
The Issue: Incorrect Product Formulation
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pointe Scientific AutoHDL/LDL Cholesterol Calibrator Recalled by Medtest...
The Issue: Vials of the autoHDL/LDL Calibrator were shipped without a vial label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contrave (naltrexone HCl and bupropion HCl) Extended-Release Tablets...
The Issue: Defective Container: Customer complaints of punctures in the bottle.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ambu Aura40 Standard Recalled by Besmed Health Business Corporation Due to...
The Issue: Ambu Aura40 Standard, Reusable Laryngeal Mask packaged in a pouch marked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Recalled...
The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HipLOC Hip Fracture Fixation System-Hiploc System 140¿ Plate 38 mm Recalled...
The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HipLOC Hip Fracture Fixation System- Hiploc System 130¿ Plate 38 Recalled by...
The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Recalled...
The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azelastine HCl Ophthalmic Solution 0.05% Recalled by Akorn, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications:out-of-specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Camber Pharmaceuticals Recalled by Hetero Labs Limited Unit V Due to CGMP...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Camber Pharmaceuticals Recalled by Hetero Labs Limited Unit V Due to CGMP...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Camber Pharmaceuticals Recalled by Hetero Labs Limited Unit V Due to CGMP...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Camber Pharmaceuticals Recalled by Hetero Labs Limited Unit V Due to CGMP...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.