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. 1,808 recalls have been distributed to Mississippi in the last 12 months.
Showing 40841–40860 of 49,744 recalls
Recalled Item: TOPIRAMATE Tablets 200 mg Recalled by Zydus Pharmaceuticals USA Inc Due to...
The Issue: Presence of Foreign Tablets: Presence of topiramate 100 mg tablets comingled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CREON (pancrelipase) Delayed-Release Capsules Recalled by AbbVie Inc Due to...
The Issue: Presence of Foreign Tablets/Capsules; Presence of co-mingled LipaCreon 13000.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips Expression Information Portal (IP5) Model 865471. The IP5 is...
The Issue: Frozen Display Numerics and Disabled Menu Keys after extended run time. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ and ADVIA Centaur¿ XP and ADVIA Centaur¿ CP Recalled by...
The Issue: Stability of the ADVIA Centaur Cleaning Solution is not assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omni Micro-electrode/ electrode for cobas b221 analyzer. The Roche...
The Issue: The default for normal values are inconsistent between cobas b 221 and other...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prescription eyeglass safety lenses. Vision correction Recalled by Eyemart...
The Issue: Prescription eyeglass safety lenses did not meet specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Ingenuity CT Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: Ingenuity CT system can mislabel the exposure that results in an image in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASSEMBLY Recalled by Intuitive Surgical, Inc. Due to Correction due to the...
The Issue: Correction due to the detection of a motor sensor failure in the Patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT Total T3 Reagent Kit (7K64) consists of: - 1 Recalled by Abbott...
The Issue: 17% of ARCHITECT Total T3 Reagent Kit, LN 7K64-20/-25 reagent lots 38901UI00...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MethylPREDNISolone TABLETS Recalled by Qualitest Pharmaceuticals Due to...
The Issue: Subpotent; 6 month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HEPARIN SODIUM Recalled by Hospira Inc. Due to Presence of Particulate...
The Issue: Presence of Particulate Matter: A particulate, confirmed as human hair, was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Roma Tomatoes Recalled by Expo Fresh L.L.C Due to Potential Salmonella...
The Issue: Expo Fresh is recalling Roma Tomatoes because they have a potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Buprenorphine Hydrochloride Injection Recalled by Hospira Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specification: Out of Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Persona The Personalized Knee System 2.5 mm Female Screw 48 Recalled by...
The Issue: The Persona 48mm X 2.5mm Female Screw is being recalled due to potential use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI¿ Pediatric Anesthesia Breathing Circuits Recalled by Teleflex...
The Issue: The pediatric breathing circuits can crack prior to and during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKenzie Perforator Drills are bone cutting and drilling instruments that...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A zipser clamp is an instrument used to compress reduce Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D'errico perforator drills are bone cutting and drilling instruments that...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Manual bunnell cranial drills are bone cutting and drilling instruments...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A circumcision clamp is an instrument used to compress the Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.