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. 1,152 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
1,152 in last 12 months

Showing 5821–5840 of 28,964 recalls

Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Bronchovideoscope Recalled by Olympus Corporation of the Americas...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Bronchovideoscope Recalled by Olympus Corporation of the Americas...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Bronchovideoscope Recalled by Olympus Corporation of the Americas...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Tracheal Intubation Fiberscope Recalled by Olympus Corporation of...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Tracheal Intubation Fiberscope Recalled by Olympus Corporation of...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 5F 100CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 8F 90CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 5F PRE-SHAPED 40 90CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 6F 90CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 6F PRE-SHAPED 40 90CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Bronchovideoscope Recalled by Olympus Corporation of the Americas...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 7F 100CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 8F PRE-SHAPED 40 90CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 8F 100CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 8F PRE-SHAPED 40 100CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 5F PRE-SHAPED 40 100CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 7F 90CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 6F 100CM MULTI PURPOSE Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 7F PRE-SHAPED 40 100CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 6F PRE-SHAPED 40 100CM Recalled by Boston...

The Issue: Stryker Neurovascular has observed that certain lots of Guider Softip XF...

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

Class II — Potential Health HazardOngoing