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. 2,644 recalls have been distributed to Iowa in the last 12 months.
Showing 4101–4120 of 28,127 recalls
Recalled Item: MIRRO MRI VR SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBALT DR MRI SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROME VR MRI SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIRRO MRI DR SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBALT VR MRI SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMO MRI DR SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIRRO MRI VR SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBALT XT HF CRT-D MRI SureScan Recalled by Medtronic Inc. Due to Potential...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVERA S VR Recalled by Medtronic Inc. Due to Potential for manufacturing...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product not distributed in the US. Implantable Cardioverter Defibrillators:...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBALT XT HF QUAD CRT-D MRI SureScan Recalled by Medtronic Inc. Due to...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROME HF QUAD CRT-D MRI SureScan Recalled by Medtronic Inc. Due to Potential...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt XT HF CDT-D MRI SureScan Recalled by Medtronic Inc. Due to Potential...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVERA MRI S DR SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMO MRI VR SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBALT XT HF QUAD CRT-D MRI SureScan Recalled by Medtronic Inc. Due to...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIRRO MRI DR SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVERA MRI S DR SureScan Recalled by Medtronic Inc. Due to Potential for...
The Issue: Potential for manufacturing defect. Weld crack led to devices failing at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Blueprint Software Recalled by Tornier S.A.S. Due to The software...
The Issue: The software bug allows for case planning with anatomic glenoid Perform /...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyoSPECT System Recalled by GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING...
The Issue: There is a potential issue regarding the service handles for the internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.