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. 2,597 recalls have been distributed to Iowa in the last 12 months.
Showing 10661–10680 of 28,127 recalls
Recalled Item: IceRod" 1.5 Cryoablation Needle Recalled by Boston Scientific Corporation...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceSphere" 1.5 Cryoablation Needle Recalled by Boston Scientific Corporation...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceFORCE" 2.1 CX 90¿ Cryoablation Needle Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Three IcePearl" 2.1 CX Prostate Cryoablation Kit Recalled by Boston...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceSphere" 1.5 90¿ Cryoablation Needle Recalled by Boston Scientific...
The Issue: Complaint trend regarding needle shaft gas leaks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENNOVATE MIS REMOVALKEY SHORT Recalled by Aesculap Implant Systems LLC Due...
The Issue: Fracture or breakage of the spinal fixation arm at the downtube instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System Recalled by...
The Issue: Zimmer Biomet is conducting a medical device correction to update the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus LS - Manual Defibrillator Recalled by Remote Diagnostic Technologies...
The Issue: A software error was detected within software version 1.3.4 for the Tempus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...
The Issue: Failure to execute the visual inspection correctly prior to locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capnostream 35 Portable Respiratory Monitor Recalled by Covidien Llc Due to...
The Issue: The firm has released software update V01.05.02.16 (also known as V1.5.2) in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contour VL Variable Length Ureteral Stent Set Recalled by Boston Scientific...
The Issue: Trace amounts of metallic debris were found on the stent related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Contour VL Variable Length Ureteral Stent Recalled by Boston Scientific...
The Issue: Trace amounts of metallic debris were found on the stent related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Mg R1 - Product Usage: For the quantitative in Recalled by Randox...
The Issue: Failing to meet the linearity performance claims quoted on the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Rx Series Mg - Product Usage: For the quantitative Recalled by Randox...
The Issue: Failing to meet the linearity performance claims quoted on the kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Intellis Spinal Cord Stimulator Recalled by Medtronic...
The Issue: A710 Intellis Clinician Application has a software issue that can result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.