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 41414160 of 28,964 recalls

Medical DeviceApril 17, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: Blood Pump Rotor Recalled by Fresenius Medical Care Holdings, Inc. Due to An...

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2024· Integra LifeSciences Corp.

Recalled Item: Integra¿ Cranial access kit (without Prep solutions) Bit and Guard- Recalled...

The Issue: Potential holes and tears in the sterile packaging (header bag) of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T BlueStar Hemodialysis Machine Recalled by Fresenius Medical Care...

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T BlueStar Hemodialysis Machine Recalled by Fresenius Medical Care...

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T BlueStar Hemodialysis Machine Recalled by Fresenius Medical Care...

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T BlueStar Hemodialysis Machine Recalled by Fresenius Medical Care...

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2024· YAMAHA MOTOR CORPORATION

Recalled Item: Optical Inspection System Recalled by YAMAHA MOTOR CORPORATION Due to...

The Issue: Non-medical laser products which were determined to not be in compliance...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2024· YAMAHA MOTOR CORPORATION

Recalled Item: Yamaha Surface Mounter YR series Recalled by YAMAHA MOTOR CORPORATION Due to...

The Issue: Non-medical laser products which were determined to not be in compliance...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2024· LeMaitre Vascular, Inc.

Recalled Item: Syntel Silicone Thrombectomy Catheter Recalled by LeMaitre Vascular, Inc....

The Issue: The guide tip can become damaged and result in the tip detaching.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2024· Cardinal Health 200, LLC

Recalled Item: CardinalHealth Curity Flexible Adhesive Bandage X-Large 2 x 3.75 in....

The Issue: Potential contamination of the product with latex adhesive residual.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2024· NRT X-RAY A/S

Recalled Item: Intelli-C: Right side suspended Tabletop Recalled by NRT X-RAY A/S Due to...

The Issue: X-ray system C-arm may experience uncontrolled motion if 1) AC motor...

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: 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: 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 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 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: 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 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: 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.

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