Product Recalls in Colorado

Product recalls affecting Colorado — including food, drugs, consumer products, medical devices, and vehicles distributed to Colorado. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,707 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,707 in last 12 months

Showing 41614180 of 28,964 recalls

Medical DeviceApril 16, 2024· Medtronic Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2024· Medtronic Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2024· Medtronic Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2024· Medtronic Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2024· Medtronic Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2024· Medtronic Inc.

Recalled Item: Cobalt XT 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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2024· Medtronic Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2024· Medtronic Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2024· Medtronic Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2024· Medtronic Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2024· Medtronic Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2024· Medtronic Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2024· Medtronic Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2024· Medtronic Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2024· Medtronic Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2024· Stryker Orthopaedics

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2024· Maquet Medical Systems USA

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2024· Stryker Orthopaedics

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2024· Philips North America Llc

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 15, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis" Anesthesia Station ES Recalled by CareFusion 303, Inc. Due to...

The Issue: Potential fluid ingress of anesthesia station or med station may result in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing