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. 2,306 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,306 in last 12 months

Showing 4284142860 of 48,326 recalls

Medical DeviceOctober 11, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT Computed Tomography X-Ray System Recalled by Philips Medical...

The Issue: If the couch, with the footrest extension attached, is positioned where the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· St. Jude Medical

Recalled Item: Safire Duo Ablation Catheter MediGuide Enabled Recalled by St. Jude Medical...

The Issue: St. Jude Medical Cardiovascular and Ablation Technologies Division is...

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

Class II — Potential Health HazardOngoing
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi eXtreme ACCELERATOR Dietary Supplement Capsules Recalled by Pure...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi AMP'D UP Advanced Weight Loss Dietary Supplement capsules Recalled...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi BTrim ULTIMATE BOOST Dietary Supplement capsules Recalled by Pure...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi BTrim MAX Dietary Supplement capsules Recalled by Pure Edge...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi INSANE Bee Pollen Dietary Supplement Capsules Recalled by Pure Edge...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi INSANE AMP'D Dietary Supplement capsules Recalled by Pure Edge...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 10, 2013· Nutrition Center, Inc. dba Nutri-West

Recalled Item: Total Enzyme Recalled by Nutrition Center, Inc. dba Nutri-West Due to...

The Issue: Nutrition Center voluntarily recalled Total Enzymes and Total Probiotics...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 10, 2013· Nutrition Center, Inc. dba Nutri-West

Recalled Item: Total Probiotics Recalled by Nutrition Center, Inc. dba Nutri-West Due to...

The Issue: Nutrition Center voluntarily recalled Total Enzymes and Total Probiotics...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 10, 2013· Cayenne Medical Inc.

Recalled Item: Drill (Fluted-Hard Bone) Recalled by Cayenne Medical Inc. Due to A review of...

The Issue: A review of complaints identified a trend for drills breaking.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: VariAx Compression Plating System Recalled by Stryker Howmedica Osteonics...

The Issue: Stryker received two reports indicating that during screw insertion under a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Nanosphere, Inc.

Recalled Item: The Verigene Enteric Pathogens Nucleic Acid Test (EP) is a multiplexed...

The Issue: Nanosphere has received several reports relating to an increased rate of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Nanosphere, Inc.

Recalled Item: The Verigene Respiratory Virus Plus Nucleic Acid Test (RV+) on Recalled by...

The Issue: Nanosphere has received several reports relating to an increased rate of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Nanosphere, Inc.

Recalled Item: The Verigene Clostridium difficile Nucleic Acid Test (CDF) is a qualitative...

The Issue: Nanosphere has received several reports relating to an increased rate of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Nanosphere, Inc.

Recalled Item: The Verigene Gram Negative Blood Culture Nucleic Acid Test (BC-GN) Recalled...

The Issue: Nanosphere has received several reports relating to an increased rate of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Nanosphere, Inc.

Recalled Item: The Verigene Gram-Positive Blood Culture Nucleic Acid Test (BC-UP) performed...

The Issue: Nanosphere has received several reports relating to an increased rate of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Mixing Cup Arrays utilized on VITROS 250 Recalled...

The Issue: Ortho Clinical Diagnostics issued a product correction notification for...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Nova Biomedical Corporation

Recalled Item: Nova StatStrip/StatSensor Hospital Blood Glucose Meter Recalled by Nova...

The Issue: Revised Battery Instructions for Removal and Expiration Date due to battery...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Mizuho America, Inc.

Recalled Item: Mizuho Sugita Titanium Standard Aneurysm Clip II Recalled by Mizuho America,...

The Issue: Specific item numbers form Lots 27-J and 29-J of Sugita T2 Aneurysm Clips....

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

Class II — Potential Health HazardOngoing