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. 2,367 recalls have been distributed to Wyoming in the last 12 months.
Showing 30361–30380 of 48,219 recalls
Recalled Item: VITROS CRP Slides: 1) VITROS¿ Chemistry Products CRP Slides (250 Recalled by...
The Issue: CRP samples diluted using VITROS Chemistry Products Specialty Diluent,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OR Table Recalled by Trumpf Medical Systems, Inc. Due to Trumpf has...
The Issue: Trumpf has identified six incidents of pinched cables.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SONNET Mini Battery Pack CableProduct Usage: The SONNET Mini Battery...
The Issue: Unit Defect: Firm inspection revealed units did not have the compartment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquilion Prime TSX-303A Aquilion PRIME is a multislice helical CT Recalled...
The Issue: Toshiba American Medical Systems (TAMS) is recalling the Aquilion CT system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit Recalled by...
The Issue: Disengaged screw head could potentially not be retained in the Torque...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Ostase Calibrators Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter has determined that the Access Ostase Calibrator and Access...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FMsealer Open Shears. Model FM3001 Recalled by Domain Surgical, Inc. Due to...
The Issue: Domain Surgical, Inc. announces a voluntary field action for the FMsealer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Ostase QC Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...
The Issue: Beckman Coulter has determined that the Access Ostase Calibrator and Access...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hyolev MB URINARY ANTISEPTIC Tablets Recalled by Burel Pharmaceuticals Inc...
The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: UROPHEN MB URINARY ANTISEPTIC Tablets Recalled by Burel Pharmaceuticals Inc...
The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: UROLET MB URINARY ANTISEPTIC Recalled by Burel Pharmaceuticals Inc Due to...
The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenazopyridine Hydrochloride Tablets Recalled by Burel Pharmaceuticals Inc...
The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AZUPHEN MB URINARY ANTISEPTIC Capsules Recalled by Burel Pharmaceuticals Inc...
The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenazopyridine Hydrochloride Tablets Recalled by Burel Pharmaceuticals Inc...
The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: URAMIT MB URINARY ANTISEPTIC Capsules Recalled by Burel Pharmaceuticals Inc...
The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Indiomin MB URINARY ANTISEPTIC Recalled by Burel Pharmaceuticals Inc Due to...
The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Chloride Ophthalmic Solution Recalled by Akorn Inc Due to Subpotent...
The Issue: Subpotent Drug: concentration of product is less than labeled amount.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ADVIA 560 Hematology Systems Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens is investigating an issue which may cause an incorrect result to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi-Med Single Lumen Catheters sold in Centurion convenience kits. The...
The Issue: The kits contain Multi-Med Single Lumen Catheters that have a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVION S250 Product Usage: Proton Radiation Therapy System Recalled by...
The Issue: Recovery of Incorrect Isocenter -operational change
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.