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. 2,383 recalls have been distributed to Wyoming in the last 12 months.
Showing 25001–25020 of 27,462 recalls
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.