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. 2,503 recalls have been distributed to Wyoming in the last 12 months.
Showing 13061–13080 of 48,219 recalls
Recalled Item: Nextra Cannulated Hammertoe Standard Instrument Kit-indicated for small bone...
The Issue: During insertion of the middle phalanx implant into bone, the driver may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LuSys 2nd Generation of COVID-19 Viral Antigen Test For all Recalled by...
The Issue: COVID-19 test kits (Antibody Rapid Test kit and Antigen Rapid Test Kit) are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COVID-19 IgG/IGM Antibody Test For Detection of COVID-19 IgG and Recalled by...
The Issue: COVID-19 test kits (Antibody Rapid Test kit and Antigen Rapid Test Kit) are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Everest MI XT Outer Dilator Recalled by K2M, Inc Due to Stryker received two...
The Issue: Stryker received two (2) complaints for units from specific lots of Inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metoprolol Succinate Extended-Release Tablets Recalled by Ascend...
The Issue: Failed Dissolution Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Recalled by TELEFLEX MEDICAL INC Due...
The Issue: The firm received reports indicating PTD tip separation during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Recalled by TELEFLEX MEDICAL INC Due...
The Issue: The firm received reports indicating PTD tip separation during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5 Fr. X 65 cm Arrow-Trerotola PTD Kit Recalled by TELEFLEX MEDICAL INC Due...
The Issue: The firm received reports indicating PTD tip separation during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device) Recalled by...
The Issue: The firm received reports indicating PTD tip separation during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device) Recalled by...
The Issue: The firm received reports indicating PTD tip separation during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Recalled by TELEFLEX MEDICAL INC Due...
The Issue: The firm received reports indicating PTD tip separation during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow-Trerotola Over-The-Wire PTD Kit Recalled by TELEFLEX MEDICAL INC Due...
The Issue: The firm received reports indicating PTD tip separation during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tretinoin Capsules Recalled by Teva Pharmaceuticals USA Due to Failed...
The Issue: Failed Dissolution Specifications; Low Out of specification (OOS) results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clobetasol Propionate Foam Recalled by Ingenus Pharmaceuticals Llc Due to...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mucus Relief D Recalled by Dr. Reddy's Laboratories, Inc. Due to Subpotent drug
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brownie Points Schmurtle 2oz Packaged in food grade cellophane only Recalled...
The Issue: Contains Statement on Label does not include all allergens - Peanuts
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RNAstill Molecular Transport Medium Vial Recalled by BASE 10 GENETICS INC...
The Issue: The product does not have 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Voyager Rollator-intended as a mechanical walker Model Number: RLEU10xx...
The Issue: Wheel spoke may crack causing the wheel to separate from the axle may result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mimvey (estradiol and norethindrone acetate tablets USP) 1 mg/0.5 mg...
The Issue: Mislabeling
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.