Product Recalls in Iowa
Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,437 recalls have been distributed to Iowa in the last 12 months.
Showing 31961–31980 of 49,990 recalls
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: 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: 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: 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: 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: 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: 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 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: 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: 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: 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.
Recalled Item: FIRST Omeprazole 2mg/mL in FIRST PPI Suspension Compounding Kit Recalled by...
The Issue: Labeling: Label error on declared strength. Package Insert -Error in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FIRST Omeprazole 2mg/mL in FIRST PPI Suspension Compounding Kit Recalled by...
The Issue: Labeling: Label error on declared strength. Package Insert -Error in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brownwood Farms Michigan Cherry Preserves 12oz glass bottles and 1 Recalled...
The Issue: Products contain milk not declared on the label.
Recommended Action: Do not consume. Return to store for a refund or discard.