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. 2,568 recalls have been distributed to Montana in the last 12 months.
Showing 2141–2160 of 27,852 recalls
Recalled Item: LAPAROSCOPY PACK Recalled by American Contract Systems Inc Due to ACS is...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAPAROSCOPY PACK Recalled by American Contract Systems Inc Due to ACS is...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TOTAL HIP PACK Recalled by American Contract Systems Inc Due to ACS is...
The Issue: ACS is unable to confirm product sterilization assurance requirements were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AURORA Surgiscope System Recalled by Integra LifeSciences Corp. Due to...
The Issue: Possibility for the obturator to break (separate).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDITECH Expanse Laboratory (LAB) Recalled by Medical Information...
The Issue: Entering multiple keys that trigger input simultaneously may remove data...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...
The Issue: the DxI 9000 encoder wheel was misaligned on the motor shaft, leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access 2 Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due to...
The Issue: Beckman Coulter identified that an issue for Access 2 Sample Motors (B48016)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aortic Root Cannula: 1. DLP Aortic Root Cannula A. CANNULA Recalled by...
The Issue: Unexpected loose material in the male luer used in the aortic root cannula...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rotarex Atherectomy System and Instructions for Use Recalled by Bard...
The Issue: Atherectomy Catheter eIFU updated to clarify and emphasize procedural steps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion System (V6 Platform) Recalled by Baxter...
The Issue: There is the potential for missing motor mounting screws, which may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Spectrum IQ Infusion System with Dose IQ Safety Software Recalled by...
The Issue: There is the potential for missing motor mounting screws, which may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelePACS (Image Fusion Module) - InteleViewer Recalled by INTELERAD...
The Issue: A software application that receives digital images and data from various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IsoLoc Short Profile Prostate Immobilization Treatment Balloon Device Kit...
The Issue: Product is mislabeled with the incorrect fill volume.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL LMW Heparin Controls Recalled by Instrumentation Laboratory Due to...
The Issue: Multiple complaints indicating lower than expected quality control (QC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS Heart Failure (HF) System that consist of: -CardioMEMS Hospital...
The Issue: Due to issues associated with data migration of patient information and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...
The Issue: The forceps have been used in ways not covered by the design resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...
The Issue: The forceps have been used in ways not covered by the design resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...
The Issue: The forceps have been used in ways not covered by the design resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...
The Issue: The forceps have been used in ways not covered by the design resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...
The Issue: The forceps have been used in ways not covered by the design resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.