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. 2,340 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,340 in last 12 months

Showing 3530135320 of 48,326 recalls

DrugSeptember 30, 2015· Premiere Sales Group

Recalled Item: Rhino 7 Platinum 3000 Recalled by Premiere Sales Group Due to Undeclared Active

The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 30, 2015· Moonstruck Chocolate Company

Recalled Item: Moonstruck Chocolates 9 piece Nuts & Chews Collection. The box Recalled by...

The Issue: Moonstruck Chocolates 9pc Nuts & Chews Collection product is recalled due to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 30, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista System (MG) Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: Erroneous low results on a small number of reagent wells. There is the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2015· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD CD3 (SK7) FITC Recalled by Becton, Dickinson and Company, BD Biosciences...

The Issue: Two lots of CD3 (SK7) FITC label contains an error in the Spanish Small text.

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

Class III — Low RiskOngoing
Medical DeviceSeptember 29, 2015· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Recalled by Stryker Howmedica Osteonics Corp. Due to...

The Issue: Stryker is recalling various lots of the Trithion MIS Modular Distal Capture...

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

Class II — Potential Health HazardOngoing
DrugSeptember 29, 2015· Fit Firm and Fabulous

Recalled Item: Ultimate Herbal Slimcap Capsules Recalled by Fit Firm and Fabulous Due to...

The Issue: Marketed Without An Approved NDA/ANDA: product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 29, 2015· Hospira Inc.

Recalled Item: Amidate (Etomidate Injection Recalled by Hospira Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification(OOS)...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 28, 2015· Perrigo Company PLC

Recalled Item: Cetirizine HCl 10 mg Tablet Recalled by Perrigo Company PLC Due to Failed...

The Issue: Failed Impurity/Degradations Specifications; impurity identified as...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 28, 2015· GE Healthcare

Recalled Item: The Centricity PACS-IW with Universal Viewer is a device that Recalled by GE...

The Issue: Inaccurate distance measurements with magnified projection X-ray images.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2015· GE Healthcare

Recalled Item: The Centricity Universal Viewer Version is a device that displays Recalled...

The Issue: Inaccurate distance measurements with magnified projection X-ray images.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Calibrator Kit 9 Calibrator Recalled by...

The Issue: The firm is conducting a product correction due to an increase in U90-382 or...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2015· Varian Medical Systems, Inc.

Recalled Item: ARIA Radiation Oncology Recalled by Varian Medical Systems, Inc. Due to An...

The Issue: An anomaly was identified with the ARIA for Radiation Oncology software with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2015· Stryker Spine

Recalled Item: Stryker Radius 5.5 to 3.5 Rod to Red Connector Recalled by Stryker Spine Due...

The Issue: Stryker Spine is recalling Radius Rod to Rod Connector 5.5 to 3.5 mm...

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

Class II — Potential Health HazardOngoing
DrugSeptember 25, 2015· Tf Supplements

Recalled Item: Rhino 7 Platinum 3000 Recalled by Tf Supplements Due to Undeclared Desmethyl

The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared desmethyl...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 25, 2015· Tf Supplements

Recalled Item: RHINO 7 3000 Recalled by Tf Supplements Due to Undeclared Desmethyl

The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared desmethyl...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 25, 2015· Medline Industries Inc

Recalled Item: ACETAMINOPHEN REGULAR-STRENGTH PAIN RELIEVER tablets Recalled by Medline...

The Issue: Labeling: Label Error on Declared Strength- Bottles containing 500 mg...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 25, 2015· Medline Industries Inc

Recalled Item: ACETAMINOPHEN EXTRA-STRENGTH PAIN RELIEVER tablets Recalled by Medline...

The Issue: Labeling: Label Error on Declared Strength- Bottles containing 500 mg...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 25, 2015· Boehringer Ingelheim Roxane Inc

Recalled Item: FUROSEMIDE Tablets USP Recalled by Boehringer Ingelheim Roxane Inc Due to...

The Issue: CGMP Deviations: The active pharmaceutical ingredient (API) intended for use...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2015· Boehringer Ingelheim Roxane Inc

Recalled Item: FUROSEMIDE Tablets USP Recalled by Boehringer Ingelheim Roxane Inc Due to...

The Issue: CGMP Deviations: The active pharmaceutical ingredient (API) intended for use...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 25, 2015· Actavis Laboratories, FL, Inc.

Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by Actavis...

The Issue: Failed Dissolution Specifications: Low Out-of-Specification results for the...

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

Class II — Potential Health HazardOngoing
Refund