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. 2,548 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,548 in last 12 months

Showing 50215040 of 48,326 recalls

Medical DeviceJune 21, 2024· Olympus Corporation of the Americas

Recalled Item: ESG-410 Electrosurgical Generator- In conjunction with electrosurgical...

The Issue: Electrosurgical Generators ESG-410 does not power on upon use, may result in...

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

Class II — Potential Health HazardOngoing
DrugJune 20, 2024· Little Moon Essentials LLC

Recalled Item: Little Moon Essentials Recalled by Little Moon Essentials LLC Due to CGMP...

The Issue: CGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2024· Little Moon Essentials LLC

Recalled Item: Little Moon Essentials Recalled by Little Moon Essentials LLC Due to CGMP...

The Issue: CGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2024· Little Moon Essentials LLC

Recalled Item: Little Moon Essentials Recalled by Little Moon Essentials LLC Due to CGMP...

The Issue: CGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2024· Little Moon Essentials LLC

Recalled Item: Little Moon Essentials Recalled by Little Moon Essentials LLC Due to CGMP...

The Issue: CGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2024· Little Moon Essentials LLC

Recalled Item: Little Moon Essentials Recalled by Little Moon Essentials LLC Due to CGMP...

The Issue: CGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2024· Little Moon Essentials LLC

Recalled Item: Little Moon Essentials Recalled by Little Moon Essentials LLC Due to CGMP...

The Issue: CGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2024· Little Moon Essentials LLC

Recalled Item: Little Moon Essentials Recalled by Little Moon Essentials LLC Due to CGMP...

The Issue: CGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 20, 2024· Little Moon Essentials LLC

Recalled Item: Little Moon Essentials Recalled by Little Moon Essentials LLC Due to CGMP...

The Issue: CGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 20, 2024· Cepheid

Recalled Item: Cepheid Recalled by Cepheid Due to Specimen collection device may leak after...

The Issue: Specimen collection device may leak after the patient sample swabs have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2024· Luminex Corporation

Recalled Item: Verigene Gram Positive Blood Culture (BC-GP) Nucleic Acid Test Recalled by...

The Issue: Potential for defective test cartridges which may result in false positive...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2024· BioFire Diagnostics, LLC

Recalled Item: BIOFIRE Blood Culture Identification 2 (BCID2) Panel Recalled by BioFire...

The Issue: If blood culture identification panel is used in conjunction with specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2024· Howmedica Osteonics Corp.

Recalled Item: UNITRAX Endoprosthesis Head Component - 43mm. Implantable component used in...

The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2024· Howmedica Osteonics Corp.

Recalled Item: UNITRAX Endoprosthesis Head Component - 38mm. Implantable component used in...

The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2024· Howmedica Osteonics Corp.

Recalled Item: UNITRAX Endoprosthesis Head Component - 42mm. Implantable component used in...

The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...

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

Class II — Potential Health HazardOngoing
DrugJune 18, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: DELFLEX PERITONEAL DIALYSIS SOLUTION With LOW MAGNESIUM / LOW CALCIUM...

The Issue: This product is being recalled due to the tube weld failure presents itself...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2024· Accord Healthcare, Inc.

Recalled Item: Dodex Injectable (Cyanocobalamin Injection) USP Recalled by Accord...

The Issue: Subpotent drug: out of specification results

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

Class III — Low RiskOngoing
Refund
DrugJune 18, 2024· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Venlafaxine Hydrochloride Recalled by The Harvard Drug Group LLC dba Major...

The Issue: Failed dissolution specifications: out of specification result obtained...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 18, 2024· Foundation Medicine, Inc.

Recalled Item: FoundationOne Companion Diagnostic (F1CDx) Recalled by Foundation Medicine,...

The Issue: Two (2) reports were sent to customers with an incorrect negative claim on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2024· Angiodynamics, Inc.

Recalled Item: SOFT-VU KUMPE 5F X 40CM -Used for patients in need Recalled by...

The Issue: Mislabeled. The shelf-box labeling (unit of sale) is accurate for the...

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

Class II — Potential Health HazardOngoing