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. 2,618 recalls have been distributed to Iowa in the last 12 months.
Showing 9541–9560 of 28,127 recalls
Recalled Item: ExacTrac Dynamic software Recalled by Brainlab AG Due to Display of...
The Issue: Display of potential patient movement might be delayed to the user for high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Heart Cath Procedure Pack Recalled by DeRoyal Industries Inc Due to...
The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Pacemaker Tray Pgybk Recalled by DeRoyal Industries Inc Due to...
The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer - multi-component system for in vitro Recalled by...
The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer- multi-component system for in vitro diagnostic...
The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer - multi-component system for in vitro Recalled by...
The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...
The Issue: Labeling does not include guidance for proper water-quality maintenance and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...
The Issue: Labeling does not include guidance for proper water-quality maintenance and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...
The Issue: Labeling does not include guidance for proper water-quality maintenance and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...
The Issue: Labeling does not include guidance for proper water-quality maintenance and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prime Fifth Wheel Stretcher-stretcher may be used for minor procedures...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proform- support surface is used to assist in the prevention Recalled by...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prime Big Wheel Stretcher-used as a short-term outpatient clinical...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S3 MedSurg Bed - intended to support and transport patients Recalled by...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Michael Graves with Stryker Highback Chair-intended for pediatric and adult...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InTouch 2131-intended to support a human patient in an acute care setting...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S3 MedSurg Bed - intended to support and transport patients Recalled by...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transport Stretcher 747 - a non-powered Recalled by Stryker Medical Division...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CUB Pediatric Crib- intended to provide a pediatric patient support Recalled...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stretcher Chair-for use in all acute care hospitals and medical Recalled by...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.