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. 2,535 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,535 in last 12 months

Showing 63216340 of 48,326 recalls

Medical DeviceFebruary 20, 2024· Boston Scientific Corporation

Recalled Item: EndoVive 20 Fr Safety PEG Push w/ENFit Kit (Box 2)-Indicated Recalled by...

The Issue: Inability to advance the guidewire through the feeding tube during placement...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2024· O&M HALYARD, INC.

Recalled Item: HALYARD SURGICAL HOOD Recalled by O&M HALYARD, INC. Due to Mislabeling

The Issue: Product was mislabeled as a Surgical Cap at its dispenser level.

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

Class III — Low RiskOngoing
DrugFebruary 20, 2024· Contract Pharmaceuticals Limited Canada

Recalled Item: Clindamycin Phosphate Topical Solution USP Recalled by Contract...

The Issue: Defective Container: Out of specification for weight due to a slow leakage...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2024· Eugia US LLC

Recalled Item: Nicardipine Hydrochloride Injection Recalled by Eugia US LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 20, 2024· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Moxifloxacin 5mg/ml Recalled by Denver Solutions, LLC DBA Leiters Health Due...

The Issue: Presence of Particulate Matter: glass vials from the manufacturer showed...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 20, 2024· Contract Pharmaceuticals Limited Canada

Recalled Item: Clindamycin Phosphate Recalled by Contract Pharmaceuticals Limited Canada...

The Issue: Defective Container: Out of specification for weight due to a slow leakage...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2024· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Moxifloxacin PF Recalled by Denver Solutions, LLC DBA Leiters Health Due to...

The Issue: Presence of Particulate Matter: glass vials from the manufacturer showed...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 20, 2024· Eugia US LLC

Recalled Item: Nicardipine Hydrochloride Injection (2.5mg/mL) Recalled by Eugia US LLC Due...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 20, 2024· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Lidocaine HCL 1% (10mg/mL) Recalled by Denver Solutions, LLC DBA Leiters...

The Issue: Presence of Particulate Matter: glass vials from the manufacturer showed...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 19, 2024· Seatex LLC

Recalled Item: 7 Eleven Hand Sanitizer Gel Recalled by Seatex LLC Due to CGMP Deviations:...

The Issue: CGMP Deviations: deficiencies were identified during an FDA inspection of...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 19, 2024· Seatex LLC

Recalled Item: PROBLEND E3 Foaming Hand Sanitizer Recalled by Seatex LLC Due to CGMP...

The Issue: CGMP Deviations: deficiencies were identified during an FDA inspection of...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 19, 2024· Seatex LLC

Recalled Item: PROBLEND Hand Sanitizer Recalled by Seatex LLC Due to CGMP Deviations:...

The Issue: CGMP Deviations: deficiencies were identified during an FDA inspection of...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 19, 2024· Seatex LLC

Recalled Item: 7 Eleven FOR GAS ISLAND USE ONLY Recalled by Seatex LLC Due to CGMP...

The Issue: CGMP Deviations: deficiencies were identified during an FDA inspection of...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 19, 2024· Seatex LLC

Recalled Item: PROBLEND Antibacterial Foaming Silk All-In-One Foaming Hand Sanitizer &...

The Issue: CGMP Deviations: deficiencies were identified during an FDA inspection of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 19, 2024· Thoratec Corp.

Recalled Item: HeartMate II Left Ventricular Assist System (LVAS): 1. HeartMate II Recalled...

The Issue: Observed outflow graft deformation known as Extrinsic Outflow Graft...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 19, 2024· ConvaTec, Inc

Recalled Item: Convatec EsteemBody Soft Convex Recalled by ConvaTec, Inc Due to Convatec...

The Issue: Convatec Inc is conducting a Voluntary Medical Device Recall (removal) for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2024· Thoratec Corp.

Recalled Item: HeartMate 3 Left Ventricular Assist System (LVAS): 1. HeartMate 3 Recalled...

The Issue: Observed outflow graft deformation known as Extrinsic Outflow Graft...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 17, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Single Use Electrosurgical Knife KD-645 Product Name: Olympus...

The Issue: A deterioration of the cutting knife, including overheating and burning, can...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: Single Use Electrosurgical Knife Product Name: Olympus Single...

The Issue: A deterioration of the cutting knife, including overheating and burning, can...

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

Class II — Potential Health HazardOngoing
DrugFebruary 16, 2024· Global Corporation

Recalled Item: Broncochem Cold & Tea (acetaminophen Recalled by Global Corporation Due to...

The Issue: Stability testing failures for one or two of the four active pharmaceutical...

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

Class II — Potential Health HazardOngoing
Refund