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 7841–7860 of 38,428 recalls

May 25, 2023· TELEFLEX LLC

Recalled Item: Flexi-Set Uncuffed Endotracheal Tube and Stylet Set

The Issue: Reports of disconnection of the 15mm connector from

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

Class I — Serious Health HazardOngoing
May 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy

The Issue: Reports of disconnection of the 15mm connector from

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

Class I — Serious Health HazardOngoing
May 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal Murphy Eye

The Issue: Reports of disconnection of the 15mm connector from

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

Class I — Serious Health HazardOngoing
May 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye

The Issue: Reports of disconnection of the 15mm connector from

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

Class I — Serious Health HazardOngoing
May 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy

The Issue: Reports of disconnection of the 15mm connector from

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

Class I — Serious Health HazardOngoing
May 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy

The Issue: Reports of disconnection of the 15mm connector from

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

Class I — Serious Health HazardOngoing
May 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal uncuffed/plain - Magill

The Issue: Reports of disconnection of the 15mm connector from

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

Class I — Serious Health HazardOngoing
May 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal Magill

The Issue: Reports of disconnection of the 15mm connector from

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

Class I — Serious Health HazardOngoing
May 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy

The Issue: Reports of disconnection of the 15mm connector from

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

Class I — Serious Health HazardOngoing
May 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal uncuffed/plain - Magill

The Issue: Reports of disconnection of the 15mm connector from

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

Class I — Serious Health HazardOngoing
May 25, 2023· TELEFLEX LLC

Recalled Item: Slick Set Uncuffed Endotracheal Tube and Stylet Set

The Issue: Reports of disconnection of the 15mm connector from

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

Class I — Serious Health HazardOngoing
May 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal uncuffed/plain - Magill

The Issue: Reports of disconnection of the 15mm connector from

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

Class I — Serious Health HazardOngoing
May 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy

The Issue: Reports of disconnection of the 15mm connector from

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

Class I — Serious Health HazardOngoing
May 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye

The Issue: Reports of disconnection of the 15mm connector from

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

Class I — Serious Health HazardOngoing
May 25, 2023· TELEFLEX LLC

Recalled Item: Slick Set Cuffed Endotracheal Tube and Stylet Set

The Issue: Reports of disconnection of the 15mm connector from

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

Class I — Serious Health HazardOngoing
May 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal uncuffed/plain - Murphy

The Issue: Reports of disconnection of the 15mm connector from

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

Class I — Serious Health HazardOngoing
May 25, 2023· TELEFLEX LLC

Recalled Item: Slick Set Uncuffed Endotracheal Tube and Stylet Set

The Issue: Reports of disconnection of the 15mm connector from

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

Class I — Serious Health HazardOngoing
May 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye

The Issue: Reports of disconnection of the 15mm connector from

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

Class I — Serious Health HazardOngoing
May 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube Murphy Eye

The Issue: Reports of disconnection of the 15mm connector from

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

Class I — Serious Health HazardOngoing
May 25, 2023· TELEFLEX LLC

Recalled Item: Slick Set Uncuffed Endotracheal Tube and Stylet Set

The Issue: Reports of disconnection of the 15mm connector from

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

Class I — Serious Health HazardOngoing