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 41181–41200 of 49,744 recalls
Recalled Item: CLAW PLATE 20mm INTERAXIS CHARLOTTE F&A SYSTEM Recalled by Wright Medical...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Gender Solution Patello-Femoral Joint (PFJ) System Patello-Femoral...
The Issue: Internal review found that five (5) PFJ implant forgings were identified as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW 3.5mm PLATE CHARLOTTE F&A SYSTEM Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Depo-Medrol (methylprednisolone acetate injectable suspension USP) Recalled...
The Issue: Failed pH Specification: A pH result of 2.9 was obtained at the 9 month...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Lack of Assurance of Sterility; complaints of mold in the overpouch
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cataflam (diclofenac potassium) tablets Recalled by Novartis Pharmaceuticals...
The Issue: Failed Tablet/Capsule Specifications: Ink identification had rubbed off...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine HCl Injection Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter: The product was discolored and contained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sunburst SUPERFOODS ORGANIC RAW CAROB POWDER in ONE POUND and Recalled by...
The Issue: The repacked product has the potential to be contaminated with Salmonella...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: OXYCODONE HYDROCHLORIDE C II Oral Solution USP Recalled by Boehringer...
The Issue: Failed Stability Specifications: Out of specification result for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD BBL Vancomycin Screen Agar Catalog number 222204 Vancomycin Screen...
The Issue: These lots of Agar may have exhibited breakthrough growth of vancomycin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Illumina Worklist Manager (IWM) (software v1.0.15) Recalled by Illumina Inc...
The Issue: A software component of the MiSeqDx instrument, called the Illumina Worklist...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RADIANCE v. 2.4X Recalled by Radiometer America Inc Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minstrel (with scale) Product Usage: is a mobile passive hoist. Recalled by...
The Issue: ArjoHuntleigh received three reports where the bolt under the scale...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSpace Portal (ISP) DX/HX/EX Recalled by Philips Medical Systems...
The Issue: The following software issues have been identified in the affected products....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUN DASH RADIUS 252 PN 8000809705. The device is intended Recalled by JK...
The Issue: The integrity of the wires inside main electrical chord become compromised...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GALT VALVED TEARAWAY KIT GALT VTI w/ Sideport Stainless Steel Recalled by...
The Issue: The adhesive used in the product could dislodge when objects are inserted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GALT VALVED TEARAWAY INTRODUCER SET GALT VTI RX ONLY UNITS Recalled by Galt...
The Issue: The adhesive used in the product could dislodge when objects are inserted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL Sleeve Installation Tool Sizes: 6mm Recalled by OrthoPediatrics Corp Due...
The Issue: Weld fractures on the Sleeve Installation Tool for ACL reconstruction system.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.