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. 2,502 recalls have been distributed to Mississippi in the last 12 months.
Showing 20621–20640 of 28,172 recalls
Recalled Item: NKII CSTI Porous Femoral NKII NP Femoral prosthesis Recalled by Zimmer...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Specify 5-6-5 Lead Recalled by Medtronic Neuromodulation Due to Some Specify...
The Issue: Some Specify 5-6-5 and 2x8 surgical lead product labeling does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bipolar Shell prosthesis Recalled by Zimmer Biomet, Inc. Due to LDPE bag...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSYS 6 INCH BEADED FC 1 prosthesis Recalled by Zimmer Biomet, Inc. Due to...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Microsystems (Schweiz) Ag. The common name of the device Recalled by...
The Issue: An electronic component of the Leica M525 OH4 and Leica M720 OH5 surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRCT MIS CR MOB PLT prosthesis Recalled by Zimmer Biomet, Inc. Due to LDPE...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CR Flex GSF Porous Femoral LPS Flex GSF Porous Femoral Recalled by Zimmer...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS-FLEX GSF OPT prosthesis Recalled by Zimmer Biomet, Inc. Due to LDPE bag...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Knee LPS Porous FEM NexGen Knee LPS Option FEM Recalled by Zimmer...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZIMMER UNI HIGH FLEX PRECOAT FEM prosthesis Recalled by Zimmer Biomet, Inc....
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gender PFJ FEMORAL COMP Recalled by Zimmer Biomet, Inc. Due to LDPE bag...
The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eclipse Treatment Planning System versions 11 Recalled by Varian Medical...
The Issue: When using PBC 11.0.31 to calculate the dose for a conventional arc field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew BEAVER Blade 4.0mm Part Number: 72203307 Orthopedic Recalled...
The Issue: Blade exhibiting fracture during hip arthroscopy procedures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX PENTRA Glucose PAP CP ref. A11A01668 reagent is intended Recalled by...
The Issue: N-Acetylcysteine (NAC) present in the blood of patients treated for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX PENTRA Triglycerides CP ref. A11A01640 is an in vitro Recalled by Horiba...
The Issue: N-Acetylcysteine (NAC) present in the blood of patients treated for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX PENTRA Uric Acid CP ref. A11A01670 is an in Recalled by Horiba...
The Issue: N-Acetylcysteine (NAC) present in the blood of patients treated for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX PENTRA Lactic Acid CP ref. A11A01721 reagent is intended Recalled by...
The Issue: N-Acetylcysteine (NAC) present in the blood of patients treated for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 25 consists of all product under product code: LPH Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 48 consists of all product under product code: JWH Recalled by...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 12 consists of all product under product code JDI Recalled by Zimmer...
The Issue: As a result of the insufficient sealer calibration data for product packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.