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. 2,271 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,271 in last 12 months

Showing 4638146400 of 48,326 recalls

FoodOctober 2, 2012· Kellogg Company

Recalled Item: Kellogg's Frosted Mini Wheats Recalled by Kellogg Company Due to This...

The Issue: This voluntary recall is initiated due to the possible presence of fragments...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 2, 2012· Kellogg Company

Recalled Item: Canadian Product: Kellogg's Mini Wheats Recalled by Kellogg Company Due to...

The Issue: This voluntary recall is initiated due to the possible presence of fragments...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 2, 2012· Kellogg Company

Recalled Item: Kellogg's Mini Wheats Recalled by Kellogg Company Due to This voluntary...

The Issue: This voluntary recall is initiated due to the possible presence of fragments...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 2, 2012· GE Healthcare It

Recalled Item: Centricity Cardio Imaging 5.0 is a software only Picture Archiving Recalled...

The Issue: GE Healthcare is aware of a potential safety risk where an image labeling...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 2, 2012· Becton Dickinson & Company

Recalled Item: Case Carton: BD Oral Dispensing Syringe 1 mL Clear with Tip Cap BD Recalled...

The Issue: BD received a complaint report for mixed syringe tips (oral and non-oral...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2012· Ebi, Llc

Recalled Item: Biomet Polaris 5.5 Button Lock Screw Inserter. Catalog number 14-500178...

The Issue: Broken screw insertor hardness was measured and found to be below the...

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

Class II — Potential Health HazardOngoing
DrugSeptember 28, 2012· ITW Dymon

Recalled Item: Lemon Hand Sanitizing Wipes [n-alkyl dimethyl benzyl ammonium chloride...

The Issue: CGMP Deviations: The products were manufactured with raw material which...

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

Class III — Low RiskOngoing
Refund
FoodSeptember 28, 2012· Fairytale Brownies, Inc

Recalled Item: Fairytale Brand Peanut Butter Sprites Recalled by Fairytale Brownies, Inc...

The Issue: The firm initiated voluntarily recall because the products contains peanut...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 28, 2012· Fairytale Brownies, Inc

Recalled Item: Fairytale Brownies Brand Peanut Butter Brownies Recalled by Fairytale...

The Issue: The firm initiated voluntarily recall because the products contains peanut...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 28, 2012· Fairytale Brownies, Inc

Recalled Item: Fairytale Brownies Brand Peanut Butter Cookies Recalled by Fairytale...

The Issue: The firm initiated voluntarily recall because the products contains peanut...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 28, 2012· Late July Snacks, LLC

Recalled Item: Late July Organic Mini Peanut Butter Sandwich Crackers packaged in Recalled...

The Issue: Organic Mini Peanut Butter Sandwich Crackers are recalled due to Sunland...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 28, 2012· Ventana Medical Systems Inc

Recalled Item: VENTANA (a member of the Roche Group) DISCOVERY ULTRA Recalled by Ventana...

The Issue: Potential for a waste fluid overflow condition to accur while running...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2012· Ventana Medical Systems Inc

Recalled Item: VENTANA (a member of the Roche Group) BenchMark ULTRA Recalled by Ventana...

The Issue: Potiential for a waste fluid overflow condition to accur while running...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Philips Medical System Extended Brilliance Workspace (EBW) Recalled by...

The Issue: Incorrect values may be displayed. Philips is issuing a software update...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2012· International Technidyne Corp.

Recalled Item: Pro Time Microcoagulation System/ Pro Time 3 Cuvette Recalled by...

The Issue: Some Pro Time3 Test Cuvettes within a specified lot range may recover lower...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2012· Philips Medical Systems (Cleveland) Inc

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

The Issue: Philips is issued a Field Change Order to update Extended Brilliance...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2012· Biomet 3i, LLC

Recalled Item: Product is Full OSSEOTITE Parallel Walled Certain Implant Recalled by Biomet...

The Issue: Biomet 3i recalled Full OSSEOTITE 2 Tapered Certain Implant and Full...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2012· Biomet 3i, LLC

Recalled Item: Product is Full OSSEOTITE 2 Tapered Certain Implant Recalled by Biomet 3i,...

The Issue: Biomet 3i recalled Full OSSEOTITE 2 Tapered Certain Implant and Full...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2012· Synthes USA HQ, Inc.

Recalled Item: Synthes External Fixation System Tube to Tube Clamp Recalled by Synthes USA...

The Issue: The insert provided with the product for the specific lot number indicates...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2012· ICU Medical, Inc.

Recalled Item: 3 PORT "OFF" MANIFOLD w/WASTE BAG Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical, Inc. has identified a potential comingling of components where...

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

Class II — Potential Health HazardOngoing