Product Recalls in New Mexico

Product recalls affecting New Mexico — including food, drugs, consumer products, medical devices, and vehicles distributed to New Mexico. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,025 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
2,025 in last 12 months

Showing 57215740 of 27,850 recalls

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· Olympus Corporation of the Americas

Recalled Item: Olympus Airway Mobilescope 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 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
Medical DeviceJuly 27, 2023· Boston Scientific Corporation

Recalled Item: Guider Softip Guide Catheter 7F 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· 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 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 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton-T1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton C1/T1/MR1 Recalled by Hamilton Medical, Inc. Due to Degrading...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton-T1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton-C1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton-MR1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Zimmer, Inc.

Recalled Item: M/L Taper Hip Prosthesis Extended Offset Recalled by Zimmer, Inc. Due to The...

The Issue: The outer package labeling and product etch are for a Size 6, however, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton-T1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 25, 2023· SenTec AG

Recalled Item: Membrane Changer Single-Use Recalled by SenTec AG Due to During rework of...

The Issue: During rework of components during the manufacturing process, an additional...

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

Class II — Potential Health HazardOngoing