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. 1,830 recalls have been distributed to Montana in the last 12 months.
Showing 20461–20480 of 27,852 recalls
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: Product 72 consists of all product code: JDI and same 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.
Recalled Item: Product 63 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 32 consists of all product under product code: HWC 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 70 consists of all product under product code: JDI 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: 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: Product 34 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: 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: 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: 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: Product 45 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 66 consists of all product under product code: JDI 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: 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: Product 17 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: 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: Product 36 consists of all product under product code: HSB 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 41 consists of all product under product code: KTT 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: 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: Product 20 consists of all prod oct under poduct code: 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.
Recalled Item: Product 47 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.