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. 2,530 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,530 in last 12 months

Showing 72217240 of 48,326 recalls

Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: 24 BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: This recall is being issued due to items within the kit have expired prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CENTRAL LINE BLOOD CULTURE DRA Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: This recall is being issued due to items within the kit have expired prior...

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

Class II — Potential Health HazardOngoing
DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Dry Eye Relief (Polyethylene Glycol 400 Recalled by Cardinal...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Eye Irritation Relief (Polyvinyl alcohol 0.5% Recalled by...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Lubricant Eye Drops (Carboxymethylcellulose Sodium Recalled by...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Polyvinyl Alcohol 1.4% Lubricating Eye Drops Recalled by The Harvard Drug...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Dry Eye Relief (Carboxymethylcellulose Sodium Recalled by...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Lubricant Eye Drops (Propylene Glycol Recalled by Cardinal...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· Cardinal Health Inc.

Recalled Item: LEADER brand Lubricant Eye Drops (Carboxymethylcellulose Sodium Recalled by...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 31, 2023· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Lubricating Tears Eye Drops (Dextran/Hypromellose) Recalled by The Harvard...

The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 31, 2023· Maquet Cardiovascular, LLC

Recalled Item: Acrobat-i Vacuum Positioner System Recalled by Maquet Cardiovascular, LLC...

The Issue: The Positioner Arm may not tighten or lock during normal use.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2023· BioReference Health, LLC

Recalled Item: The 4Kscore Test Recalled by BioReference Health, LLC Due to Mathematical...

The Issue: Mathematical modeling of the 4Kscore with and without DRE information was...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2023· KENT IMAGING, INC.

Recalled Item: Snapshot NIR Recalled by KENT IMAGING, INC. Due to Tissue oxygenation...

The Issue: Tissue oxygenation measurement system touchscreens may be unresponsive,...

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

Class II — Potential Health HazardOngoing
DrugOctober 27, 2023· NCS Healthcare of Kentucky Inc

Recalled Item: Lisinopril Tablets USP 20 mg Recalled by NCS Healthcare of Kentucky Inc Due...

The Issue: Presence of Foreign Tablets: Potential of stray tablet(s) of Amlodipine...

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

Class III — Low RiskOngoing
Refund
DrugOctober 27, 2023· NCS Healthcare of Kentucky Inc

Recalled Item: Buspirone Hydrochloride Tabs USP 10 mg Recalled by NCS Healthcare of...

The Issue: Presence of Foreign Tablets: Potential of stray tablet(s) of Amlodipine...

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

Class III — Low RiskOngoing
Refund
DrugOctober 27, 2023· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Extended Phenytoin Sodium Capsules Recalled by Amneal Pharmaceuticals of New...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 26, 2023· VistaPharm LLC

Recalled Item: Mycophenolate Mofetil for Oral Suspension Recalled by VistaPharm LLC Due to...

The Issue: Defective Container: The adaptor does not fit into the neck of the bottle...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 26, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 250-Intended for...

The Issue: RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 400-Intended for...

The Issue: RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 750-Intended for...

The Issue: RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the...

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

Class II — Potential Health HazardOngoing