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. 2,533 recalls have been distributed to Iowa in the last 12 months.
Showing 17721–17740 of 28,127 recalls
Recalled Item: GE Healthcare Discovery IQ X-ray system Recalled by GE Healthcare, LLC Due...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT660 Recalled by GE Healthcare, LLC Due to It was...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare BrightSpeed X-ray system Recalled by GE Healthcare, LLC Due to...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery Ml DR X-ray system Recalled by GE Healthcare, LLC...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT520 X-ray system Recalled by GE Healthcare, LLC Due...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery PET/CT 600 Recalled by GE Healthcare, LLC Due to It...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare lnnova IGS 540 ACT X-ray system Recalled by GE Healthcare, LLC...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CT580 Recalled by GE Healthcare, LLC Due to It was...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare LightSpeed VCT X-ray system Recalled by GE Healthcare, LLC Due...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery NM/CT 670. 670 Pro Recalled by GE Healthcare, LLC...
The Issue: It was discovered that an issue has been identified that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuikClot TraumaPad Recalled by Z-Medica, LLC Due to Packaging breach may...
The Issue: Packaging breach may compromise sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENTARAY NAV High-Density Mapping Catheter. Recalled by Biosense Webster,...
The Issue: Contraindication language updated in the Instructions For Use (IFU) to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENTARAY NAV High-Density Mapping Catheter. Recalled by Biosense Webster,...
The Issue: Contraindication language updated in the Instructions For Use (IFU) to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis Vibe Systems with Software Version VD10B Recalled by Siemens Medical...
The Issue: Software error. In Sensis Vibe systems with software version VD10B, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter Synchron AQUA CAL Level 1 Recalled by Beckman Coulter Inc...
The Issue: The firm identified a negative shift of 5mmol/L for sodium recovery in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multiphor II Electrophoresis System GE HealthCare Product Number: 18-1018-06...
The Issue: Potential for electric shock in the case of a failure to install the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS Testosterone Recalled by bioMerieux, Inc. Due to Complaints were...
The Issue: Complaints were received from customers observing falsely overestimate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD¿ High Volume Administration Set with FlowStop Recalled by Smiths...
The Issue: One lot of CADD¿ High Volume Administration sets, part number 21-7381-24,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MesaLabs Conductivity Standard Solution Recalled by Mesa Laboratories, Inc....
The Issue: Mesa Laboratories is recalling Conductivity/TDS Calibrator Solution due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DigitalDiagnost 3.1.x X-Ray System Recalled by Philips Electronics...
The Issue: During recent evaluations of the Philips DigitalDiagnost 3.1.x, we have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.