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. 985 recalls have been distributed to Iowa in the last 12 months.
Showing 37461–37480 of 49,990 recalls
Recalled Item: Westbrook's Horseradish Dilly Beans Recalled by Westbrook's Cannery Due to...
The Issue: Products potentially underprocessed.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: WESTBROOK'S CANNERY HOT DILL PICKLES Recalled by Westbrook's Cannery Due to...
The Issue: Products potentially underprocessed.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Westbrook's Hot Dilly Beans Recalled by Westbrook's Cannery Due to Products...
The Issue: Products potentially underprocessed.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: WESTBROOK'S CANNERY HORSERADISH DILL PICKLES Recalled by Westbrook's Cannery...
The Issue: Products potentially underprocessed.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: WESTBROOK'S CANNERY DILL PICKLES Recalled by Westbrook's Cannery Due to...
The Issue: Products potentially underprocessed.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: West brook's Dilly Beans Recalled by Westbrook's Cannery Due to Products...
The Issue: Products potentially underprocessed.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nitroglycerin Transdermal System 0.4 mg/hr (18 cm2) Recalled by Kremers...
The Issue: Failed Impurities/Degradation Specifications: Two lots failed specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength Analgesic Thera-Gesic Pain Relieving Creme Relief from:...
The Issue: Subpotent Drug: menthol and methyl salicylate below specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SENSE Body Coil 1.5T with identification Recalled by Philips Electronics...
The Issue: Wrong positioning of the coil cables can create unintended resonances via...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Potential...
The Issue: Potential issue leading to data loss and patient data mix-up
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infant Heel Warmer and Infant Gel Warmer Recalled by CooperSurgical, Inc....
The Issue: Product marketed without a 510(k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Actuator for angiographic x-ray monitor ceiling suspension system. Actuator...
The Issue: The actuator assembly became detached and the monitor carriage with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: nordicICE v 2.3.14 nordicICE is an image processing software package...
The Issue: The bug causes BOLD activation maps to be visualized as overlays without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slip-Cath Beacon Tip Catheter. Angiographic catheter. For use in...
The Issue: Reports of catheter tip splits and or separation. Loss of device function,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beacon Tip Royal Flush Plus High-Flow Catheter. Angiographic catheter. For...
The Issue: Reports of catheter tip splits and or separation. Loss of device function,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beacon Tip Torcon NB Advantage Catheter. Angiographic catheter. For use...
The Issue: Reports of catheter tip splits and or separation. Loss of device function,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Silhouette Lift brochure Silhouette Sutures are for use in midface Recalled...
The Issue: Silhouette Lift is recalling the Silhouette Suture brochure because it does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spirit One A-C Powered Hospital Bed Recalled by Stryker Medical Division of...
The Issue: Customer complaints associated with faulty brake system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spirit One A-C Powered Hospital Bed Recalled by Stryker Medical Division of...
The Issue: Inaccurate scale systems
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVS SUGAR FREE BLACK CHERRY COUGH DROPS (MENTHOL-COUGH SUPPRESSANT) Recalled...
The Issue: Presence of Foreign Tablets/Capsules: Presence of comingled Sugar Free Honey...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.