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. 2,410 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,410 in last 12 months

Showing 2022120240 of 48,326 recalls

DrugAugust 29, 2019· Johnson Matthey Inc.

Recalled Item: Oxaliplatin Active Pharmaceutical Ingredient Recalled by Johnson Matthey...

The Issue: cGMP Deviations: Potential glass contamination

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 29, 2019· LABSTYLE INNOVATIONS

Recalled Item: Dario Blood Glucose Monitoring System Recalled by LABSTYLE INNOVATIONS Due...

The Issue: The Dario-Blood Glucose Tracker Android App versions 4.3.0-4.3.2 may...

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

Class II — Potential Health HazardOngoing
DrugAugust 28, 2019· AVKARE Inc.

Recalled Item: AVKARE Fexofenadine Hydrochloride Tablets USP Antihistamine 180 mg Recalled...

The Issue: Failed Stability Specifications.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 28, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion CIRCLAMP W/1.3 CM BELL-single-use Recalled by Centurion Medical...

The Issue: A mismatch between the angle of the hole in the base and the angle of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: cobas c 701 and 702 Analyzer/Module-RF interference claims for the Recalled...

The Issue: Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion CIRCLAMP W/1.1CM BELL - single-use Recalled by Centurion Medical...

The Issue: A mismatch between the angle of the hole in the base and the angle of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: cobas c 311 Recalled by Roche Diagnostics Operations, Inc. Due to Tina-quant...

The Issue: Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for...

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

Class II — Potential Health HazardOngoing
DrugAugust 27, 2019· American Health Packaging

Recalled Item: Lamivudine Tablets Recalled by American Health Packaging Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Package Insert; an error in the Dosage Forms...

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

Class III — Low RiskOngoing
Refund
FoodAugust 26, 2019· Hometown Food Company

Recalled Item: Martha White Gluten Free Sweet Yellow Cornbread & Muffin Mix Recalled by...

The Issue: Product tested positive for gluten but is labeled as Gluten free

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 26, 2019· Natures One Inc

Recalled Item: PediaSmart Organic Soy Vanilla Beverage Mix Recalled by Natures One Inc Due...

The Issue: Undeclared milk allergen.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 26, 2019· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Positron Emission Tomograpy and Computed Tomography System Recalled by...

The Issue: Potential sporadic software bugs in R001.3.0.0.750505 software version may...

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

Class II — Potential Health HazardOngoing
DrugAugust 24, 2019· Tuscano and Delucia Group (DBA Entropic Labs)

Recalled Item: Entropic Labs SARM RAD-140 Recalled by Tuscano and Delucia Group (DBA...

The Issue: Marketed Without An Approved NDA/ANDA: product contains Selective Androgen...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: fexofenadine hydrochloride tablets USP Recalled by Aurolife Pharma, LLC Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Fexofenadine Hydrochloride Tablets USP Recalled by Aurolife Pharma, LLC Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Wal-Fex (Fexofenadine Hydrochloride) Tablets USP Recalled by Aurolife...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Allergy (Fexofenadine Hydrochloride) Tablets USP Recalled by Aurolife...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Fexofenadine HCL Tablets USP Recalled by Aurolife Pharma, LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Allergy Relief (fexofenadine hydrochrloride) tablets Recalled by Aurolife...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Allergy (Fexofenadine Hydrochloride) Tablets USP Recalled by Aurolife...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2019· Aurolife Pharma, LLC

Recalled Item: Fexofenadine Hydrochloride Tablets USP Recalled by Aurolife Pharma, LLC Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund