Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,285 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,285 in last 12 months

Showing 4380143820 of 48,219 recalls

Medical DeviceJune 16, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: The SurgiCounter Charging Cradle Product Usage: SurgiCounter Charging...

The Issue: Faulty SurgiCounter Charging Cradle can prevent the scanner from charging or...

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
FoodJune 14, 2013· See's Candies Inc.

Recalled Item: See's Dark Raisins: Ingredients: Raisins Recalled by See's Candies Inc. Due...

The Issue: Potential for nuts and/or nut and egg residue may be present in some of the...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 14, 2013· See's Candies Inc.

Recalled Item: See's Milk Raisins: Ingredients: Raisins Recalled by See's Candies Inc. Due...

The Issue: Potential for nuts and/or nut and egg residue may be present in some of the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 14, 2013· PIONEER SURGICAL TECHNOLOGY, INC.

Recalled Item: Streamline MIS Spinal Fixation System Fixed Rod Holder NON STERILE Recalled...

The Issue: The affected fixed rod holders did not allow the instrument to lock down on...

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
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
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