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. 2,622 recalls have been distributed to Iowa in the last 12 months.
Showing 7841–7860 of 28,127 recalls
Recalled Item: HAMILTON-C6 Intensive Care Ventilator Recalled by Hamilton Medical AG Due to...
The Issue: Ventilator status indicator board can become loose, which could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-Stream Irrigation System (Catalog No. 5551000) and X-Stream Irrigation...
The Issue: The device may potentially cause a fire, leading to a safety risk.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Genesis II Non-Porous Tibial Baseplate Size 5 Right Recalled by Smith &...
The Issue: The product was mispackaged (swapped). The devices within the inner tray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroLift System Recalled by Neotract Inc Due to There is the potential that...
The Issue: There is the potential that during implant deployment, the device may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Sprinter OTW Recalled by Medtronic Inc Due to Luer has balloon...
The Issue: Luer has balloon diameter printed as "2.25mmx12mm" instead of the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 2.3mm Tapered Router Recalled by Stryker Instruments Due to There is...
The Issue: There is a potential for the core diameter to be undersized, which may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZEISS Axio Observer 5 microscope Recalled by Zeiss, Carl Inc Due to An...
The Issue: An incorrect Unique Device Identification (UDI) label was installed on some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Premier magnetic resonance scanner Recalled by GE Healthcare, LLC Due...
The Issue: Under rare conditions, SIGNA Premier gradient coils could result in elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom PRO+ 36" MRS Surface With X-Ray mattress Recalled by Baxter...
The Issue: The failure mode on the affected mattresses can cause a reduction in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom PRO+ MRS Surface For Versacare With X-Ray mattress Recalled by...
The Issue: The failure mode on the affected mattresses can cause a reduction in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom Centrella Pro+ 40" Surface mattress Recalled by Baxter Healthcare...
The Issue: The failure mode on the affected mattresses can cause a reduction in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom Centrella Pro+ 36" Surface mattress Recalled by Baxter Healthcare...
The Issue: The failure mode on the affected mattresses can cause a reduction in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom Centrella Pro+ 36" Surface With X-Ray mattress Recalled by Baxter...
The Issue: The failure mode on the affected mattresses can cause a reduction in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom PRO+ MRS Surface For Versacare mattress Recalled by Baxter...
The Issue: The failure mode on the affected mattresses can cause a reduction in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom PRO+ 36" MRS Surface mattress Recalled by Baxter Healthcare...
The Issue: The failure mode on the affected mattresses can cause a reduction in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ambra PACS Recalled by DICOM Grid, Inc. d/b/a Ambra Health Due to A race...
The Issue: A race condition between the storage system and services database has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KY JELLY LUBRICANT 2 FL OZ Recalled by Family Dollar Stores, Llc. Due to...
The Issue: Affected product was not appropriately stored in temperature-controlled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FIRST RESPONSE 2 CT Recalled by Family Dollar Stores, Llc. Due to Affected...
The Issue: Affected product was not appropriately stored in temperature-controlled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CURAD STRNG WATRPRF STRIP 1IN 20CT Recalled by Family Dollar Stores, Llc....
The Issue: Affected product was not appropriately stored in temperature-controlled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLEAR EYES CONTCT LENS DRPS LBRCTNG .5FO Recalled by Family Dollar Stores,...
The Issue: Affected product was not appropriately stored in temperature-controlled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.