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. 2,284 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,284 in last 12 months

Showing 4392143940 of 48,326 recalls

Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
DrugJune 14, 2013· Boehringer Ingelheim Roxane Inc

Recalled Item: Prednisone Tablet USP Recalled by Boehringer Ingelheim Roxane Inc Due to...

The Issue: Labeling: Missing Label; missing label on blister card

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

Class III — Low RiskOngoing
Refund
DrugJune 13, 2013· CareFusion 213, LLC

Recalled Item: ChloraPrep With Tint Recalled by CareFusion 213, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility; Immediate product pouches may not be...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 13, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Varicam/VG and VG Hawkeye devices Product Usage: The Recalled...

The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 13, 2013· Becton Dickinson & Co.

Recalled Item: BD Affirm VPIII Microbial Identification Tests Recalled by Becton Dickinson...

The Issue: In vitro diagnostic test kit may exhibit invalid internal negative control...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2013· GE Healthcare, LLC

Recalled Item: Elscint APEX Helix Recalled by GE Healthcare, LLC Due to GE became aware of...

The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 13, 2013· GE Healthcare, LLC

Recalled Item: Discovery NM/CT 670 dual detector free-geometry integrated nuclear imaging...

The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 13, 2013· GE Healthcare, LLC

Recalled Item: Optima NM/CT 640 Product Usage: The GE Optima NM/CT 640 Recalled by GE...

The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 13, 2013· GE Healthcare, LLC

Recalled Item: Discovery NM 630 Recalled by GE Healthcare, LLC Due to GE became aware of an...

The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 13, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Infinia Hawkeye 4 Option For Dual-Head Variable Angle Gamma...

The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 13, 2013· GE Healthcare, LLC

Recalled Item: Brivo NM615 Recalled by GE Healthcare, LLC Due to GE became aware of an...

The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 12, 2013· Accelerated Care Plus Corporation

Recalled Item: Omnicycle Elite Recalled by Accelerated Care Plus Corporation Due to An...

The Issue: An anomaly in the firmware that may cause Omnicycle Elite to operate at a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes CMF Distraction System The product is intended for use Recalled by...

The Issue: The firm initiated a voluntary recall of the BC Distractor Body which is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2013· Physio Control, Inc.

Recalled Item: The LIFEPAK 500 Automated External Defibrillator is a semi-automatic...

The Issue: The LIFEPAK 500 Automated External Defibrillator (AED) could be susceptible...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products PHYT Slides packaged as 90 slides/pack catalog...

The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...

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

Class II — Potential Health HazardOngoing