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. 2,365 recalls have been distributed to Mississippi in the last 12 months.
Showing 44781–44800 of 49,744 recalls
Recalled Item: Ranitidine Hydrochloride Tablets Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Microbial Contamination of Non-Sterile Products: A lot of raw material used...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Juno DRF System. Mobile X-ray system These are general Recalled by Villa...
The Issue: It has been discovered that the Air Kerma rate information is inconsistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEST Slim Recalled by CTV Best Group Due to Undeclared Drug
The Issue: Marketed without an Approved NDA/ANDA: Product contains an undeclared drug,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Benztropine Mesylate Injection Recalled by Nexus Pharmaceuticals Inc Due to...
The Issue: Presence of particulate matter: characterized as thin colorless flakes that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mavik¿ trandolapril tablets 4mg Recalled by AbbVie Inc. Due to Labeling:...
The Issue: Labeling: Incorrect Package Insert; product packaged with outdated version...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Breaded Recalled by Gourmet Express Marketing, Inc. Due to Packages of...
The Issue: Packages of breaded shrimp failed to declare shellfish (shrimp) and wheat...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Raw Pistachio Halves Recalled by Superior Nut Co. Inc. Due to Potential...
The Issue: Positive laboratory result for Salmonella sp. Speciation in progress.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Synthes Soft Tissue Retractor Small Extendible. Offset blade facilitates...
The Issue: The small extendible Soft Tissue Retractor was recalled due to locking nut...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAVIS-EX Recalled by Nidek Inc Due to Under certain circumstances, the Left...
The Issue: Under certain circumstances, the Left eye image may be saved as the Right...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00 4309-049-00 Trabecular Metal Reverse Shoulder Glenosphere Distractor Rx...
The Issue: Zimmer is initiating a lot specific recall of the Trabecular Metal" Reverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BuPROPion Hydrochloride Extended-Release Tablets (XL) Recalled by Actavis...
The Issue: Failed Dissolution Specifications: Dissolution test results at 8 hour...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leica BIOSYSTEMS Recalled by Leica Biosystems Newcastle Ltd. Due to The...
The Issue: The affected lots of the product may contain a contaminant of fungus that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Large Buttress Compression Nut For Blade Guide Sleeve TFN The Recalled by...
The Issue: The Large Buttress Compression Nut For Blade Guide Sleeve TFN was recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Tensioning Device The Synthes Osteogenesis System Recalled by...
The Issue: All lots of the Synthes Tensioning Device were recalled due to the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slipped Capital Femoral Epiphysis System Product Usage: Intended for...
The Issue: There is a possibility for the Guide Wires of the Slipped Capital Femoral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4 and 2.7 MM Locking Screw SLF-TPNG with T8 Stardrive Recalled by Synthes...
The Issue: Specific lots of the SS 2.4mm and SS 2.7mm Locking Screw (self-tapping) due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Matrix Threaded Persuader Deformity is a comprehensive thoracolumbar...
The Issue: Synthes became aware that during a procedure using the Matrix Threaded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIPELINE LS ACCESS SYSTEM Recalled by DePuy Spine, Inc. Due to Dilators and...
The Issue: Dilators and Holding Clip are being used for a secondary function of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.