Product Recalls in Montana
Product recalls affecting Montana — including food, drugs, consumer products, medical devices, and vehicles distributed to Montana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,349 recalls have been distributed to Montana in the last 12 months.
Showing 34141–34160 of 48,326 recalls
Recalled Item: NexGen LPS Flex Option Femoral NexGen LPS Flex Precoat Femoral prosthesis...
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 LPS-FLEX Option Femoral NexGen LPS-FLEX Precoat Femoral prosthesis...
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 Precoat Fem Natural Knee GSF NP Flex Recalled by Zimmer Biomet,...
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: CPT 12/14 COCR 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 CR Porous FEM NexGen Knee CR Precoat FEM prosthesis Recalled by...
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 VERSYS 6 INCH BEADED Recalled by Zimmer Biomet,...
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 CR-FLEX Option FEM NexGen CR-FLEX Precoat FEM NexGen CR-FLEX Recalled...
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: 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: CPT 12/14 COCR 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: ABX PENTRA Enzymatic Creatinine CP ref. A11A01907 reagent is intended...
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: The ABX PENTRA Cholesterol CP ref. A11A01634 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: VERSYS 7.5 INCH BEADED FC 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: 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: 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: 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: 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: 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: 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.