Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,002 recalls have been distributed to Wyoming in the last 12 months.
Showing 5761–5780 of 48,219 recalls
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: 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: 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 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: 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: EVERA MRI S 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: COBALT 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: COBALT XT 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: 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 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: 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: 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: 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: 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: Total Knee Arthroplasty (TKA) 2 Recalled by Stryker Orthopaedics Due to...
The Issue: Application software intended to be deployed on Mako 3.0, part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOHELP-i System. Blood oxygenation and carbon dioxide removal system....
The Issue: The firm identified that the measured patient leakage current in some...
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.
Recalled Item: Incisive CT - Computed Tomography X-Ray System intended to produce Recalled...
The Issue: Metal mounting box on the rotating scanner on rotor (heat change box)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.