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. 2,573 recalls have been distributed to Wyoming in the last 12 months.
Showing 2121–2140 of 48,219 recalls
Recalled Item: KIMMTRAK (tebentafusp-tebn) Injection Recalled by IMMUNOCORE, LLC Due to...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BostonSight SCLERAL Lens Recalled by Boston Foundation For Sight Due to...
The Issue: Select orders of lenses were manufactured with errors impacting sagittal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BostonSight PROSE Lens. Recalled by Boston Foundation For Sight Due to...
The Issue: Select orders of lenses were manufactured with errors impacting sagittal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry...
The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry...
The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products CHE Slides Recalled by Ortho-Clinical Diagnostics,...
The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products CHE Slides (Japan) Recalled by Ortho-Clinical...
The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torflex Transseptal Guiding Sheath Kit (TFK-M) TF85-32-63-45 TORFLEX 8.5F...
The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaCross Access Solution (VXSK) Recalled by Boston Scientific Corporation...
The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaCross RF Wire (VXW). Indicated for creation of an atrial Recalled by...
The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaCross Transseptal Sheath Kit (VXS) Product Description/IDs VXS0201 VXS...
The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: --- Shell Eggs Recalled by August Egg Company Due to Potential Salmonella...
The Issue: Potential contamination with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Orajel Baby Recalled by Church & Dwight Inc Due to Microbial Contamination...
The Issue: Microbial Contamination of Non-Sterile Products: Fungal contamination of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZICAM COLD REMEDY MEDICATED NASAL SWABS Recalled by Church & Dwight Inc Due...
The Issue: Microbial Contamination of Non-Sterile Products: Fungal contamination of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZICAM NASAL ALLCLEAR Recalled by Church & Dwight Inc Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products: Fungal contamination of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Superion IDS Kit Superion Indirect Decompression System 8MM Recalled by...
The Issue: As a result of a comprehensive product performance review it was determine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Manifold Kit: Recalled by Merit Medical Systems, Inc. Due to High...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Tubing Kit: Recalled by Merit Medical Systems, Inc. Due to High...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: High Pressure Tubing: Recalled by Merit Medical Systems, Inc. Due to High...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Waste Management Kit: Recalled by Merit Medical Systems, Inc. Due to...
The Issue: High pressure tubing may relax over time causing it to partially separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.