Medical Device Recalls

This is our largest category by volume. The FDA tracks recalls for an enormous range of medical devices: implants, pacemakers, insulin pumps, surgical tools, blood glucose monitors, X-ray machines, prosthetics, contact lenses, and home health equipment, among many others. We have records dating back to 2005 and add new ones as the FDA publishes them.

Device recalls can happen because of software bugs, manufacturing defects, bacterial contamination, incorrect labeling, or design flaws that lead to inaccurate results or equipment failure. Class I recalls are the most serious and mean the device could cause injury or death.

38,428 total recalls
0 this month

Showing 13841–13860 of 38,428 recalls

November 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number R1076709 - Product Usage:

The Issue: issues with ventilator navigation ring interface and

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

Class II — Potential Health HazardOngoing
November 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1053618 - Product Usage:

The Issue: issues with ventilator navigation ring interface and

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

Class II — Potential Health HazardOngoing
November 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1053614 - Product Usage:

The Issue: issues with ventilator navigation ring interface and

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

Class II — Potential Health HazardOngoing
November 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1053615 - Product Usage:

The Issue: issues with ventilator navigation ring interface and

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

Class II — Potential Health HazardOngoing
November 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1076716 - Product Usage:

The Issue: issues with ventilator navigation ring interface and

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

Class II — Potential Health HazardOngoing
November 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1137292 - Product Usage:

The Issue: issues with ventilator navigation ring interface and

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

Class II — Potential Health HazardOngoing
November 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1076717 - Product Usage:

The Issue: issues with ventilator navigation ring interface and

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

Class II — Potential Health HazardOngoing
November 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number R1053618 - Product Usage:

The Issue: issues with ventilator navigation ring interface and

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

Class II — Potential Health HazardOngoing
November 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V680 Ventilator Part Number 850011 - Product Usage:

The Issue: issues with ventilator navigation ring interface and

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

Class II — Potential Health HazardOngoing
November 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage:

The Issue: issues with ventilator navigation ring interface and

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

Class II — Potential Health HazardOngoing
November 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Plus Ventilator Part Number 1138747 - Product

The Issue: issues with ventilator navigation ring interface and

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

Class II — Potential Health HazardOngoing
November 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1076709 - Product Usage:

The Issue: issues with ventilator navigation ring interface and

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

Class II — Potential Health HazardOngoing
November 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number DU1053617 - Product Usage:

The Issue: issues with ventilator navigation ring interface and

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

Class II — Potential Health HazardOngoing
November 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Plus Ventilator Part Number 1137276 - Product

The Issue: issues with ventilator navigation ring interface and

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

Class II — Potential Health HazardOngoing
November 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1053616 - Product Usage:

The Issue: issues with ventilator navigation ring interface and

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

Class II — Potential Health HazardOngoing
November 2, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1053617 - Product Usage:

The Issue: issues with ventilator navigation ring interface and

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

Class II — Potential Health HazardOngoing
November 2, 2020· Smith & Nephew, Inc.

Recalled Item: Bone fixation nail. TRIGEN INTERTAN - Product Usage: indicated for

The Issue: Manufacturing packaging error

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

Class II — Potential Health HazardTerminated
November 2, 2020· Chromsystems Instruments & Chemicals GmbH

Recalled Item: MassChrom Amino Acid Analysis Plasma Control Level I

The Issue: Products do not meet stability criteria and may

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

Class II — Potential Health HazardTerminated
November 2, 2020· Chromsystems Instruments & Chemicals GmbH

Recalled Item: 3PLUS1 Multilevel Plasma Calibrator Set

The Issue: Products do not meet stability criteria and may

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

Class II — Potential Health HazardTerminated
November 2, 2020· Chromsystems Instruments & Chemicals GmbH

Recalled Item: MassChrom Amino Acid Analysis Plasma Control Level III

The Issue: XXX

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

Class II — Potential Health HazardTerminated