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. 2,524 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,524 in last 12 months

Showing 1050110520 of 48,326 recalls

Medical DeviceNovember 7, 2022· Cordis US Corp

Recalled Item: Cordis Angiographic Catheter Extensions. Used to transport fluid from the...

The Issue: There is a potential for separation at the male connector.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2022· Getinge Usa Sales Inc

Recalled Item: Flow-c Anesthesia System (Product Code 6887700) Flow-e Anesthesia System...

The Issue: The power backup battery, under certain conditions, may exhibit reduced...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugNovember 5, 2022· Adam's Polishes LLC

Recalled Item: Adam's Polishes ALCOHOL BASED HAND SANITIZER Recalled by Adam's Polishes LLC...

The Issue: CGMP Deviations: Other lots of hand sanitizer are being recalled because...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 5, 2022· Adam's Polishes LLC

Recalled Item: Adam's Polishes ALCOHOL BASED HAND SANITIZER Recalled by Adam's Polishes LLC...

The Issue: Chemical Contamination: FDA analysis found 1 lot of Adam's Polishes ALCOHOL...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 4, 2022· Medical Action Industries, Inc. 306

Recalled Item: Medical Action INDUSTRIES INC. Port a Cath Kit Recalled by Medical Action...

The Issue: XXX

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests Japan...

The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests (600T)-...

The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests OUS...

The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2022· Olympus Corporation of the Americas

Recalled Item: HF Resection Electrodes Recalled by Olympus Corporation of the Americas Due...

The Issue: An incompatible HF cable may be packaged with the HF Resection Electrodes....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2022· Icotec Ag

Recalled Item: VADER Pedicle System Torque Wrench Recalled by Icotec Ag Due to During...

The Issue: During internal testing (at manufacturer site) of two torque wrench devices,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· SynCardia Systems LLC

Recalled Item: SynCardia Total Artificial Heart System (70CC): 500101-001 SynCardia Total...

The Issue: Due to tears reported tears in the cannula due to wear and tear stress.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...

The Issue: Medical and surgical procedure trays and kits underwent certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: STRADIS HEALTHCARE Recalled by Stradis Medical, LLC dba Stradis Healthcare...

The Issue: Medical and surgical procedure trays and kits underwent certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: STRADIS HEALTHCARE Recalled by Stradis Medical, LLC dba Stradis Healthcare...

The Issue: Medical and surgical procedure trays and kits underwent certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...

The Issue: Medical and surgical procedure trays and kits underwent certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: STRADIS HEALTHCARE Recalled by Stradis Medical, LLC dba Stradis Healthcare...

The Issue: Medical and surgical procedure trays and kits underwent certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...

The Issue: Medical and surgical procedure trays and kits underwent certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...

The Issue: Medical and surgical procedure trays and kits underwent certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: STRADIS HEALTHCARE Recalled by Stradis Medical, LLC dba Stradis Healthcare...

The Issue: Medical and surgical procedure trays and kits underwent certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...

The Issue: Medical and surgical procedure trays and kits underwent certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing