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.
Showing 4701–4720 of 38,428 recalls
Recalled Item: SIGNA 7.0T
The Issue: GE HealthCare has become aware that for certain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.0T SIGNA HDxt Family
The Issue: GE HealthCare has become aware that for certain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Victor
The Issue: GE HealthCare has become aware that for certain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MR950
The Issue: GE HealthCare has become aware that for certain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Artist
The Issue: GE HealthCare has become aware that for certain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Hero
The Issue: GE HealthCare has become aware that for certain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Premier
The Issue: GE HealthCare has become aware that for certain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA MAGNUS
The Issue: GE HealthCare has become aware that for certain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5T SIGNA HDxt Family
The Issue: GE HealthCare has become aware that for certain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Prime
The Issue: GE HealthCare has become aware that for certain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Pioneer
The Issue: GE HealthCare has become aware that for certain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MR750w 3.0T
The Issue: GE HealthCare has become aware that for certain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brivo MR355
The Issue: GE HealthCare has become aware that for certain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusor Space Product Name: Perfusor Space Syringe Pump
The Issue: Perfusor Space Syringe Pump's instructions for use previously
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusor Space Product Name: Perfusor PCA Syringe Pump
The Issue: Perfusor Space Syringe Pump's instructions for use previously
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusor Space Product Name: PERFUSOR SPACE ACM-KIT Model/Catalog
The Issue: Perfusor Space Syringe Pump's instructions for use previously
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusor Space Product Name: Perfusor Space Infusion Pump
The Issue: Perfusor Space Syringe Pump's instructions for use previously
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusor Space Product Name: Perfusor Space Syringe Pump
The Issue: Perfusor Space Syringe Pump's instructions for use previously
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury
The Issue: The tiller separates from the base/front caster assembly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury
The Issue: The tiller separates from the base/front caster assembly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.