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. 2,542 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,542 in last 12 months

Showing 54415460 of 48,326 recalls

DrugMay 10, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Rizatriptan Benzoate Tablets USP Recalled by Glenmark Pharmaceuticals Inc.,...

The Issue: CGMP Deviations: N-Nitroso Desmethyl Rizatriptan Impurity results that are...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 10, 2024· Bryant Ranch Prepack, Inc.

Recalled Item: Cephalexin for Oral Suspension Recalled by Bryant Ranch Prepack, Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Back label states Each contains:...

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

Class III — Low RiskOngoing
Refund
FoodMay 10, 2024· Healthwest Minerals, Inc. dba Mt. Capra Products

Recalled Item: Mt. Capra Goat Milk Formula Recipe Kit (net wt. 10lbs. Recalled by...

The Issue: The Goat Milk Formula Recipe Kit has been sold and marketed as infant...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugMay 10, 2024· Bryant Ranch Prepack, Inc.

Recalled Item: Cephalexin for Oral Suspension Recalled by Bryant Ranch Prepack, Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Back Label states 'Each contains:...

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

Class III — Low RiskOngoing
Refund
DrugMay 10, 2024· Bryant Ranch Prepack, Inc.

Recalled Item: Cephalexin for Oral Suspension Recalled by Bryant Ranch Prepack, Inc. Due to...

The Issue: Labeling: Not Elsewhere Classified: Back Label states 'Each contains:...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 10, 2024· LEICA BIOSYSTEMS NUSSLOCH GMBH

Recalled Item: Leica HistoCore Arcadia H Recalled by LEICA BIOSYSTEMS NUSSLOCH GMBH Due to...

The Issue: An issue with safe usage of the device was identified whereby toxic smoke...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Sol-Millennium Medical Inc.

Recalled Item: Syringe Tip Caps labeled as: 1) SOL-M Syringe Tip Cap Recalled by...

The Issue: Products in distribution were found by FDA to be to be substantially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Sol-Millennium Medical Inc.

Recalled Item: Syringes with Fixed Needles labeled as: a) SOL-M: 1) SOL-M Recalled by...

The Issue: Products in distribution were found by FDA to be to be substantially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Sol-Millennium Medical Inc.

Recalled Item: Syringes with exchangeable needles labeled as: SOL-CARE: 1) SOL-CARE 10ml...

The Issue: Products in distribution were found by FDA to be to be substantially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Sol-Millennium Medical Inc.

Recalled Item: Syringes with Low Dead Space labeled as: a) SOL-M 1ml Recalled by...

The Issue: Products in distribution were found by FDA to be to be substantially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Sol-Millennium Medical Inc.

Recalled Item: Syringes with Luer Slip Tips labeled as: 1) SOL-M 1ml Recalled by...

The Issue: Products in distribution were found by FDA to be to be substantially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Sol-Millennium Medical Inc.

Recalled Item: Syringes with Eccentric Tips labeled as: 1) SOL-M 10ml Eccentric Recalled by...

The Issue: Products in distribution were found by FDA to be to be substantially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· First Source Inc

Recalled Item: First Source Vision M. Portable cart and platform that supports Recalled by...

The Issue: Potential for the bolt that secures the positioning arm to the gas spring to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· C.R. Bard Inc

Recalled Item: Bard Medical SureStep Foley Tray System Recalled by C.R. Bard Inc Due to...

The Issue: Some of the devices may function incorrectly resulting in no temperature...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Stryker GmbH

Recalled Item: Stryker Hoffman LRF Wire Tensioner Recalled by Stryker GmbH Due to The...

The Issue: The adjustment ring on the device may become loose resulting in the wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· Remote Diagnostic Technologies Ltd.

Recalled Item: Philips Tempus LS-Manual Defibrillator Recalled by Remote Diagnostic...

The Issue: Simultaneous ECG measurements with multiple devices, including a manual...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 9, 2024· First Source Inc

Recalled Item: First Source iQ Flex M. Portable cart and platform that Recalled by First...

The Issue: Potential for the bolt that secures the positioning arm to the gas spring to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2024· Baxter Healthcare Corporation

Recalled Item: Centrella Max - The Centrella Smart+ Bed is intended for Recalled by Baxter...

The Issue: There is a potential for the top cover of the hospital bed mattress to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2024· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Immunodiagnostic Products Vitamin B12 Range Verifier - In vitro...

The Issue: The results generated by the VITROS Immunodiagnostic Products Vitamin B12...

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

Class III — Low RiskOngoing
Medical DeviceMay 8, 2024· Thoratec Corp.

Recalled Item: Thoratec HeartMate System Monitor Recalled by Thoratec Corp. Due to System...

The Issue: System monitor screen may display atypical behavior: Overlapping...

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

Class I — Serious Health HazardOngoing