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. 1,191 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
1,191 in last 12 months

Showing 1001–1020 of 51,434 recalls

DrugOctober 22, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: clomiPRAMINE Hydrochloride Recalled by Zydus Pharmaceuticals (USA) Inc Due...

The Issue: cGMP deviations: an observed Out of Specification of Nitrosamine Drug...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat Recalled by Olympus Corporation of the Americas Due to...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2025· Olympus Corporation of the Americas

Recalled Item: Olympus Thunderbeat 5 mm Recalled by Olympus Corporation of the Americas Due...

The Issue: Firm is initiating a removal due to continued reports of adverse events.

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

Class II — Potential Health HazardOngoing
DrugOctober 22, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: clomiPRAMINE Hydrochloride Recalled by Zydus Pharmaceuticals (USA) Inc Due...

The Issue: cGMP deviations: an observed Out of Specification of Nitrosamine Drug...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 22, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: clomiPRAMINE Hydrochloride Recalled by Zydus Pharmaceuticals (USA) Inc Due...

The Issue: cGMP deviations: an observed Out of Specification of Nitrosamine Drug...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 21, 2025· Kenvue Brands LLC

Recalled Item: TYLENOL Recalled by Kenvue Brands LLC Due to Defective Container

The Issue: Defective Container

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 21, 2025· Medtronic MiniMed, Inc.

Recalled Item: CareLink Clinic Recalled by Medtronic MiniMed, Inc. Due to Software error...

The Issue: Software error causing incorrect data to be displayed on the 24-hour Sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2025· Accriva Diagnostics, Inc.

Recalled Item: VerifyNow PRUTest Platelet Reactivity Test UDI-DI code: 10711234150078...

The Issue: Due to an device without a premarket clearance being incorrectly package and...

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

Class III — Low RiskOngoing
DrugOctober 21, 2025· Bristol-Myers Squibb Company

Recalled Item: Opdualag (nivolumab and relatlimab-rmbw) injection Recalled by Bristol-Myers...

The Issue: Lack of Assurance of Sterility.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 20, 2025· Golden State Medical Supply Inc.

Recalled Item: NIACIN Extended-Release Tablets Recalled by Golden State Medical Supply Inc....

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund