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. 2,277 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,277 in last 12 months

Showing 4556145580 of 48,326 recalls

FoodFebruary 14, 2013· Custom Co-Pak, LLC

Recalled Item: Long Life Premium Organic Green Tea with Lemongrass Recalled by Custom...

The Issue: Recall is being conducted based on a finding of possible contamination by...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 14, 2013· Zimmer, Inc.

Recalled Item: Zimmer Patient Helper Bed Frame Adapter Assembly The bed frame Recalled by...

The Issue: The bed frame adapter assemblies may have a weak weld where the patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2013· Becton Dickinson & Company

Recalled Item: BD Vacutainer C&S Transfer Straw Kit C&S Preservative Plus Urine Tube. 4.0...

The Issue: The BD Vacutainer Urinalysis Transfer Straw Kit #364991, Lot 1335484 has...

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

Class III — Low RiskOngoing
DrugFebruary 13, 2013· Watson Laboratories Inc

Recalled Item: ZARAH¿ Drospirenone/ Ethinyl Estradiol Tablets Recalled by Watson...

The Issue: Failed Tablet/Capsule Specification; tablet breakage while pushing through...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 13, 2013· Glenmark Generics Inc., USA

Recalled Item: Montelukast Sodium Tablets Recalled by Glenmark Generics Inc., USA Due to...

The Issue: Chemical Contamination: The recall has been initiated based on multiple...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 13, 2013· Actavis Elizabeth LLC

Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...

The Issue: Failed Dissolution Specification: This product recall is due to the product...

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

Class III — Low RiskOngoing
Refund
FoodFebruary 13, 2013· Saratoga Therapeutics, LLC

Recalled Item: ebA*(TM) Multivitamin Supplement Recalled by Saratoga Therapeutics, LLC Due...

The Issue: The recall was initiated due to discovery of the presence of milk components...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 12, 2013· OLAAX International

Recalled Item: MAXILOSS Weight Advanced Recalled by OLAAX International Due to Marketed...

The Issue: Marketed Without an Approved NDA/ANDA: product contains sibutramine, a...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 12, 2013· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Irrigation Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: There is a potential for the solution to...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 12, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Intellispace Portal (ISP) Philips Medical Systems (Cleveland) Recalled by...

The Issue: Philips was notified of a problem using the IntelliSpace Portal with...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Beckman Coulter Inc.

Recalled Item: Access Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is initiating a recall due to a defective newly released...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Polymedco, Inc

Recalled Item: Test Strips packaged in the OC-Light Manual iFOBT Kit Recalled by Polymedco,...

The Issue: The test strips in the affected product lots of the OC Light immunological...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Beckman Coulter Inc.

Recalled Item: Access 2 Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is initiating a recall due to a defective newly released...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Polymedco, Inc

Recalled Item: Test Strips packaged in the OC-Light Manual iFOBT Kit Recalled by Polymedco,...

The Issue: The test strips in the affected product lots of the OC Light immunological...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Beckman Coulter Inc.

Recalled Item: UniCel DxC 600i Synchron Access Clinical System Recalled by Beckman Coulter...

The Issue: Beckman Coulter is initiating a recall due to a defective newly released...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Beckman Coulter Inc.

Recalled Item: Synchron LXi 725 Clinical System Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter is initiating a recall due to a defective newly released...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Integra LifeSciences Corp.

Recalled Item: Integra(R) Jarit(R) Monopolar Cable (Catalogue No. 600-290). For use in...

The Issue: Addendum to the Instructions for Use. The addendum emphasizes the warnings...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2013· Oculus Innovative Sciences Inc

Recalled Item: Atrapro Antipruritic Hydrogel Recalled by Oculus Innovative Sciences Inc Due...

The Issue: Out of specification result - stability test failure of free available...

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

Class II — Potential Health HazardOngoing
DrugFebruary 11, 2013· Jubilant Cadista Pharmaceuticals Inc.

Recalled Item: Pantoprazole Sodium Delayed Release Tablets USP Recalled by Jubilant Cadista...

The Issue: cGMP Deviations: Oral products were not manufactured in accordance with Good...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 11, 2013· Innominata Dba Genbio

Recalled Item: ANTI-BORRELIA (LYME) MICROPLATE EIA Kit Recalled by Innominata Dba Genbio...

The Issue: Multiple incidents of low-reacting assay plates.

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

Class II — Potential Health HazardOngoing