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 21141–21160 of 38,428 recalls

April 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA" 45mm Gray Curved Tip Articulating Vascular Reload with

The Issue: Device may be missing a sled component. The

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

Class II — Potential Health HazardTerminated
April 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA" 30mm Gray Curved Tip Articulating Vascular Reload with

The Issue: Device may be missing a sled component. The

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

Class II — Potential Health HazardTerminated
April 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX KIT1095V KIT OBESITAS (Item Code KIT1095V) Product Usage: The

The Issue: Device may be missing a sled component. The

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

Class II — Potential Health HazardTerminated
April 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 30mm -

The Issue: Device may be missing a sled component. The

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

Class II — Potential Health HazardTerminated
April 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX VWR ZESTAW DO VATS KLIN Product Usage: The Endo

The Issue: Device may be missing a sled component. The

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

Class II — Potential Health HazardTerminated
April 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA" 30mm Gray Curved Tip Articulating Vascular Reload with

The Issue: Device may be missing a sled component. The

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

Class II — Potential Health HazardTerminated
April 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1)BOX PST04089 SLEEVE AIWA CLINIC Item Number:PST04089 SLEEVE AIWA CLINIC

The Issue: Device may be missing a sled component. The

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

Class II — Potential Health HazardTerminated
April 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX VATS1SCDX DO ZABIEGOW VATS Product Usage: The Endo GIA

The Issue: Device may be missing a sled component. The

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

Class II — Potential Health HazardTerminated
April 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 45mm- 3.5mm(

The Issue: Device may be missing a sled component. The

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

Class II — Potential Health HazardTerminated
April 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX VMIN ZESTAW DO VATS PODSTAWOWY Product Usage: The Endo

The Issue: Device may be missing a sled component. The

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

Class II — Potential Health HazardTerminated
April 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX KITDE0108 BYPASS KIT LUEBECK ( KITDE0108) Product Usage: The

The Issue: Device may be missing a sled component. The

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

Class II — Potential Health HazardTerminated
April 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1)KIT4184 APEN LOBECTOMY KIT X0 Item Number: KIT4184 APEN LOBECTOMY

The Issue: Device may be missing a sled component. The

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

Class II — Potential Health HazardTerminated
April 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: KIT-DE-0080 BYPASS KIT LOHNE X1( Item KIT-DE-0080) Product Usage: The

The Issue: Device may be missing a sled component. The

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

Class II — Potential Health HazardTerminated
April 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1) BOX KITDE0143 BYPASS BOX (Item Number: KITDE0143

The Issue: Device may be missing a sled component. The

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

Class II — Potential Health HazardTerminated
April 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: BOX MGBGLOGX1 ZESTAW MINI GASTRIC BYPASS Product Usage: The Endo

The Issue: Device may be missing a sled component. The

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

Class II — Potential Health HazardTerminated
April 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: (1)BOX SLEEVEGK3 (2) BOX SLEEVEGK4 SLEEVE GASTRECTOMY (3)BOX SLEEVEJAWI SLEEVE

The Issue: Device may be missing a sled component. The

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

Class II — Potential Health HazardTerminated
April 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 60mm -2.5mm

The Issue: Device may be missing a sled component. The

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

Class II — Potential Health HazardTerminated
April 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: Endo GIA" Auto Suture" Universal Articulating Loading Unit 30mm -

The Issue: Device may be missing a sled component. The

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

Class II — Potential Health HazardTerminated
April 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: SLEEVEGK1 ZESTAW DO ZABIEGOW SLEEVEX1 Product Usage: The Endo GIA

The Issue: Device may be missing a sled component. The

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

Class II — Potential Health HazardTerminated
April 26, 2018· COVIDIEN MEDTRONIC

Recalled Item: KIT00486R OBESIDAD D. WORWARLD 2 X1 (Item Number KIT00486R) Product

The Issue: Device may be missing a sled component. The

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

Class II — Potential Health HazardTerminated