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 33381–33400 of 38,428 recalls

April 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 4"x6" Reorder Number:

The Issue: Pouch holding sterile inflation assembly and inflation adapter

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

Class II — Potential Health HazardTerminated
April 24, 2014· Cenorin, LLC

Recalled Item: HLD Systems Model 610 Washer/High Level Disinfector. Maximum weight of

The Issue: Cenorin LLC is voluntarily recalling HLD Systems Model

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

Class II — Potential Health HazardTerminated
April 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Composix" LP with Echo PS" 6x10 Reorder Number: 0144610 Indicated

The Issue: Pouch holding sterile inflation assembly and inflation adapter

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

Class II — Potential Health HazardTerminated
April 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 8"x10" Reorder Number:

The Issue: Pouch holding sterile inflation assembly and inflation adapter

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

Class II — Potential Health HazardTerminated
April 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 12"x14" Reorder Number:

The Issue: Pouch holding sterile inflation assembly and inflation adapter

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

Class II — Potential Health HazardTerminated
April 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Bard¿ Composix" LIP Mesh with Echo PS" 7"x9" Reorder Number:

The Issue: Pouch holding sterile inflation assembly and inflation adapter

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

Class II — Potential Health HazardTerminated
April 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Composix" LP with Echo PS" 10x13 HUXH0294 HUXL0314 Indicated for

The Issue: Pouch holding sterile inflation assembly and inflation adapter

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

Class II — Potential Health HazardTerminated
April 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Bard¿Ventralight" ST Mesh with Echo PS" 10"x13" Reorder Number: 5955113

The Issue: Pouch holding sterile inflation assembly and inflation adapter

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

Class II — Potential Health HazardTerminated
April 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Composix" LP with Echo PS" 6x8 Reorder Number: 0144680 Indicated

The Issue: Pouch holding sterile inflation assembly and inflation adapter

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

Class II — Potential Health HazardTerminated
April 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 6"x10" Reorder Number:

The Issue: Pouch holding sterile inflation assembly and inflation adapter

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

Class II — Potential Health HazardTerminated
April 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Bard¿ Composix" LIP Mesh with Echo PS" 8"x10" Reorder Number:

The Issue: Pouch holding sterile inflation assembly and inflation adapter

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

Class II — Potential Health HazardTerminated
April 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 6"x8" Reorder Number:

The Issue: Pouch holding sterile inflation assembly and inflation adapter

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

Class II — Potential Health HazardTerminated
April 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 6" CircleReorder Number:

The Issue: Pouch holding sterile inflation assembly and inflation adapter

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

Class II — Potential Health HazardTerminated
April 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 8" Circle Number:

The Issue: Pouch holding sterile inflation assembly and inflation adapter

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

Class II — Potential Health HazardTerminated
April 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 4.5" Circle Reorder

The Issue: Pouch holding sterile inflation assembly and inflation adapter

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

Class II — Potential Health HazardTerminated
April 24, 2014· Davol, Inc., Subs. C. R. Bard, Inc.

Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS TM 7"x9" Reorder

The Issue: Pouch holding sterile inflation assembly and inflation adapter

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

Class II — Potential Health HazardTerminated
April 24, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Aera magnetic resonance system. Indicated for use as a

The Issue: Siemens discovered a processing error for the MAGNETOM

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

Class II — Potential Health HazardTerminated
April 24, 2014· Mar Cor Purification

Recalled Item: Mar Cor Purification

The Issue: Mar Cor Purification manufactured Central Water Plant (CWP)

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

Class II — Potential Health HazardTerminated
April 23, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: e.cam camera system. Emission Computed Tomography System used to detect

The Issue: Siemens Medical Solutions USA, Inc. has received reports

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

Class II — Potential Health HazardTerminated
April 23, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: Symbia E camera system. Emission Computed Tomography System used to

The Issue: Siemens Medical Solutions USA, Inc. has received reports

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

Class II — Potential Health HazardTerminated