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. 2,551 recalls have been distributed to Iowa in the last 12 months.
Showing 16421–16440 of 49,990 recalls
Recalled Item: Fresh Thyme Taco Dip Recalled by J & J Distributing Company Due to Potential...
The Issue: Products may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Haug Fresh Taco Tray Recalled by J & J Distributing Company Due to Potential...
The Issue: Products may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Earthgrown Mini Taco Dip Recalled by J & J Distributing Company Due to...
The Issue: Products may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Caribou Coffee Turkey Sandwich Recalled by J & J Distributing Company Due to...
The Issue: Products may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Taco Platter [Kwik Trip] Recalled by J & J Distributing Company Due to...
The Issue: Products may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: tastebuds Layered Fiesta Taco Dip Recalled by J & J Distributing Company Due...
The Issue: Products may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Electrolit Fruit Punch Zero Recalled by Laboratorios Pisa Sa De Cv Due to...
The Issue: Product contains undeclared FD&C Red No. 40.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Electrolit Ponche/Fruit Punch Recalled by Laboratorios Pisa Sa De Cv Due to...
The Issue: Product contains undeclared FD&C Red No. 40.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Old Cape Cod Soup and Chowder Oyster Crackers - 8oz Box Recalled by...
The Issue: Product may contain hard plastic foreign object.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Alaris Pump Module Recalled by STEP-HAR MEDICAL LLC Due to Bezel repair...
The Issue: Bezel repair parts used, not by the original manufacturer, to service and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Patient Manual for HeartWare HVAD System. Recalled...
The Issue: IFU and Patient Manual updated to describe HVAD Controller Connection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Patient Manual for HeartWare HVAD System. Recalled...
The Issue: IFU and Patient Manual updated to describe Expected Alarm Duration. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Patient Manual for HeartWare HVAD System. Recalled...
The Issue: Medtronic HeartWare HVAD System Instructions for Use (IFU) and Patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Corporation Due to Their is a potential that...
The Issue: Their is a potential that Video Processor/Illuminators may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panther Fusion Tube Tray Recalled by Hologic, Inc Due to There is a...
The Issue: There is a potential for tube trays to leak which could potentially result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CF Delivery Dev Caps Bravo x5 Recalled by Covidien Llc Due to The capsule...
The Issue: The capsule may fail to attach to the esophageal mucosa, which in turn may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRAVO PH CAPS DELIVERY DEV5-PK Recalled by Covidien Llc Due to The capsule...
The Issue: The capsule may fail to attach to the esophageal mucosa, which in turn may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Interventional Fluoroscopic X-Ray System - Product Usage: developed for...
The Issue: Siemens has become aware of a potential issue in which the imaging system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIRE DIAGNOSTICS FenomPro SN ***** - Product Usage: a portable Recalled by...
The Issue: Erroneously high FeNO levels which may contribute to premature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyberKnife Treatment Delivery System - Product Usage: indicated for...
The Issue: The set screws that connect the Standard Treatment Couch linkage arm to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.