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 22621–22640 of 38,428 recalls

October 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 22300

The Issue: The Better Bladder device provided as part of

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

Class II — Potential Health HazardTerminated
October 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 27610 ECC PACK 3/8

The Issue: The Better Bladder device provided as part of

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

Class II — Potential Health HazardTerminated
October 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 22301

The Issue: The Better Bladder device provided as part of

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

Class II — Potential Health HazardTerminated
October 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 33700 ECC 3/8" PACK

The Issue: The Better Bladder device provided as part of

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

Class II — Potential Health HazardTerminated
October 19, 2017· Datascope Corporation

Recalled Item: Adult ECC Pack BEQ-TOP 22300

The Issue: The Better Bladder device provided as part of

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

Class II — Potential Health HazardTerminated
October 19, 2017· Datascope Corporation

Recalled Item: BO-TOP 13901 RAPID RESPONSE

The Issue: The Better Bladder device provided as part of

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

Class II — Potential Health HazardTerminated
October 19, 2017· Datascope Corporation

Recalled Item: ECC Small - Respiratory BEQ-TOP 5210

The Issue: The Better Bladder device provided as part of

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

Class II — Potential Health HazardTerminated
October 19, 2017· Datascope Corporation

Recalled Item: BO-TOP 20700 SMALL PATIENT 3/8

The Issue: The Better Bladder device provided as part of

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

Class II — Potential Health HazardTerminated
October 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 5210 ECC Set - Respiratory

The Issue: The Better Bladder device provided as part of

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

Class II — Potential Health HazardTerminated
October 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 38900 ECC PACK

The Issue: The Better Bladder device provided as part of

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

Class II — Potential Health HazardTerminated
October 19, 2017· Datascope Corporation

Recalled Item: BEQ-T 25502 1/4 Better Bladder

The Issue: The Better Bladder device provided as part of

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

Class II — Potential Health HazardTerminated
October 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 49101 Childrens Large ECC Pack

The Issue: The Better Bladder device provided as part of

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

Class II — Potential Health HazardTerminated
October 19, 2017· Datascope Corporation

Recalled Item: NICU ECC Pack BEQ-TOP 39202

The Issue: The Better Bladder device provided as part of

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

Class II — Potential Health HazardTerminated
October 19, 2017· Datascope Corporation

Recalled Item: BO-TOP 20705 SMALL PATIENT 1/4

The Issue: The Better Bladder device provided as part of

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

Class II — Potential Health HazardTerminated
October 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 41201 ECC 3/8 PUMP PAC

The Issue: The Better Bladder device provided as part of

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

Class II — Potential Health HazardTerminated
October 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 24500 ADULT ECC

The Issue: The Better Bladder device provided as part of

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

Class II — Potential Health HazardTerminated
October 19, 2017· Datascope Corporation

Recalled Item: BEQ-T 9410 Lurie Chldns Small 1/4

The Issue: The Better Bladder device provided as part of

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

Class II — Potential Health HazardTerminated
October 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 25500 ECC 3/8 w/QiD

The Issue: The Better Bladder device provided as part of

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

Class II — Potential Health HazardTerminated
October 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 24202 ADULT ECC

The Issue: The Better Bladder device provided as part of

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

Class II — Potential Health HazardTerminated
October 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 40700 HUNTINGTON

The Issue: The Better Bladder device provided as part of

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

Class II — Potential Health HazardTerminated