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. 2,498 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,498 in last 12 months

Showing 1348113500 of 48,326 recalls

Medical DeviceNovember 19, 2021· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Instructions for Use for all model numbers of the Medtronic Recalled by...

The Issue: There have been reports of stent migration.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2021· Philips North America Llc

Recalled Item: Philips Allura Xper FD series with Software Version Number: 2.1.x- Recalled...

The Issue: Set screws securing the two gliding rods of the Extra Monitors (called 7th...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH 930 Analyzer with Software version: V1.25.1 and lower- An...

The Issue: (1)Software (SW) versions V1.25.1 and lower may result in TDef (Test...

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

Class II — Potential Health HazardOngoing
DrugNovember 17, 2021· Blistex Inc

Recalled Item: Odor-Eaters Spray Powder Recalled by Blistex Inc Due to Chemical...

The Issue: Chemical contamination: Presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 17, 2021· Sandoz Inc

Recalled Item: Enoxaparin Sodium Injection Recalled by Sandoz Inc Due to Temperature Abuse;...

The Issue: Temperature Abuse; temperature excursion during shipping

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 17, 2021· Luminex Corporation

Recalled Item: ARIES HSV 1&2 Assay Recalled by Luminex Corporation Due to Impacted lot may...

The Issue: Impacted lot may leak inside the ARIES instrument. Testing confirmed a leak...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2021· Stanley Security Solutions Inc

Recalled Item: Senior Living Arial Emergency and Nurse Call Systems Recalled by Stanley...

The Issue: Systems are not alarming due to increased memory consumption.

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

Class II — Potential Health HazardOngoing
FoodNovember 16, 2021· Mountain Meadow Herbs, Inc.

Recalled Item: Mountain Meadow Herbs Brand Candida Flush Endotoxin Cleans3 Recalled by...

The Issue: Product bottle has potential to become pressurized over time. When consumer...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 16, 2021· Roche Molecular Systems, Inc.

Recalled Item: cobas LiatSystem Recalled by Roche Molecular Systems, Inc. Due to Roche has...

The Issue: Roche has identified a small number of cobas Liat analyzer units that have...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2021· Ohio Medical Corporation

Recalled Item: Instavac Portable Suction Pump Recalled by Ohio Medical Corporation Due to...

The Issue: Increase in premature device failures

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2021· Abbott

Recalled Item: Ultimum HEMOSTASIS INTRODUCER 5f 1.67 MM Recalled by Abbott Due to As a...

The Issue: As a result of a manufacturing error, one (1) lot of Ultimum Hemostasis...

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

Class II — Potential Health HazardOngoing
DrugNovember 15, 2021· Aurobindo Pharma USA Inc.

Recalled Item: Carvedilol Tablets Recalled by Aurobindo Pharma USA Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 15, 2021· Datascope Corp.

Recalled Item: Cardiosave Rescue IntraAortic Balloon Pump. Model Numbers: 0998-00-0800-75...

The Issue: Firm is initiating a correction due to the possibility of fluid ingress....

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2021· Datascope Corp.

Recalled Item: Cardiosave Hybrid IntraAortic Balloon Pump. Model Numbers: 0998-00-0800-31...

The Issue: Firm is initiating a correction due to the possibility of fluid ingress....

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

Class I — Serious Health HazardOngoing
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: PHENYLephrine HCl Recalled by SterRx, LLC Due to Lack of Assurance of Sterility

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: Succinylcholine Chloride Injection Recalled by SterRx, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: Sodium Bicarbonate in 5% Dextrose Injection Recalled by SterRx, LLC Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: Midazolam in 0.9% Sodium Chloride Injection Recalled by SterRx, LLC Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: Morphine Sulfate in 5% Dextrose Injection Recalled by SterRx, LLC Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: dilTIAZem HCl 125 mg per 125 mL (1 mg per mL) in 0.7% Sodium Chloride...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund