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. 2,387 recalls have been distributed to Montana in the last 12 months.
Showing 23761–23780 of 48,326 recalls
Recalled Item: Permobil powered wheelchairs Recalled by Permobil, Ab Due to This correction...
The Issue: This correction decision has been made because of a potential failure of one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci S/Si EndoWrist 8mm Monopolar Curved Scissors Model No. Recalled by...
The Issue: Monopolar Curved Scissor (MCS) instruments may be susceptible to developing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci X/Xi EndoWrist 8mm Monopolar Curved Scissors Model No. Recalled by...
The Issue: Monopolar Curved Scissor (MCS) instruments may be susceptible to developing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Megestrol Acetate Oral Suspension Recalled by Mckesson Corporation Due to...
The Issue: Supterpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan Tablets Recalled by AVKARE Inc. Due to CGMP Deviations: Carcinogen...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan Tablets Recalled by AVKARE Inc. Due to CGMP Deviations: Carcinogen...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan Tablets Recalled by AVKARE Inc. Due to CGMP Deviations: Carcinogen...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan Tablets Recalled by AVKARE Inc. Due to CGMP Deviations: Carcinogen...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem HCl Extended-release Capsules Recalled by Mylan Institutional,...
The Issue: Failed Impurities/Degradation Specifications; out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TECOTHERM NEO Recalled by Tec Com Gmbh Due to The action is being initiated...
The Issue: The action is being initiated due to potential installation of faulty...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTIO 15000 STORAGE MODULE Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTIO RACK INPUT MODULE Recalled by Siemens Healthcare Diagnostics, Inc. Due...
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLAB CORE UNIT / LYNX WITH IOM Recalled by Siemens Healthcare...
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTIO INPUT/OUTPUT MODULE Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLAB - STORAGE MODULE 9000 Recalled by Siemens Healthcare Diagnostics,...
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STREAMLAB - STORAGE MODULE 15000 Recalled by Siemens Healthcare Diagnostics,...
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTIO RACK OUTPUT MODULE Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTIO 9000 STORAGE MODULE Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTIO CENTRIFUGE MODULE Recalled by Siemens Healthcare Diagnostics, Inc. Due...
The Issue: The modules may have been shipped without a warning label for potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portable Suction Pump Recalled by Ohio Medical Corporation Due to The...
The Issue: The care-e-vac(R)3 Battery/AC Powered Portable Aspirator battery terminal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.