Product Recalls in Minnesota
Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,439 recalls have been distributed to Minnesota in the last 12 months.
Showing 36841–36860 of 52,120 recalls
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: 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: 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: Stree Overlord Recalled by R Thomas Marketing, LLC Due to Marketed Without...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Black Ant King Recalled by R Thomas Marketing, LLC Due to Marketed Without...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Plant Vigra Recalled by R Thomas Marketing, LLC Due to Marketed Without An...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Man King Recalled by R Thomas Marketing, LLC Due to Marketed Without An...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bull Recalled by R Thomas Marketing, LLC Due to Marketed Without An Approved...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Samurai-X Recalled by R Thomas Marketing, LLC Due to Marketed Without An...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Night Man Recalled by R Thomas Marketing, LLC Due to Marketed Without An...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Happy Passengers Recalled by R Thomas Marketing, LLC Due to Marketed Without...
The Issue: Marketed Without An Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.