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 13381–13400 of 38,428 recalls
Recalled Item: SD-210U-25 ELECTROSURGICAL SNARE
The Issue: Inspection confirmed a small percentage of sterile packages
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEEDLEMASTER 4MMx 23G UPPER
The Issue: Inspection confirmed a small percentage of sterile packages
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NA-411D-1321 ASPIRATION NEEDLE
The Issue: Inspection confirmed a small percentage of sterile packages
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAJ-244 SINGLE USE 30MM REPLACEMENT BASKET
The Issue: Inspection confirmed a small percentage of sterile packages
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX UP 2.8MMCH 23G 5MM
The Issue: Inspection confirmed a small percentage of sterile packages
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NA-601D-1519 ASPIRATION NEEDLE
The Issue: Inspection confirmed a small percentage of sterile packages
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX LOWER 23G 4MM
The Issue: Inspection confirmed a small percentage of sterile packages
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B-V443Q-A 3-LUMEN EXTRACTION BALLOON V
The Issue: Inspection confirmed a small percentage of sterile packages
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX LOWER 25G 2.5MM
The Issue: Inspection confirmed a small percentage of sterile packages
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRESCENT SNARE
The Issue: Inspection confirmed a small percentage of sterile packages
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEEDLEMASTER 3MMx 23G LOWER
The Issue: Inspection confirmed a small percentage of sterile packages
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SD-240U-10 ELECTROSURGICAL SNARE
The Issue: Inspection confirmed a small percentage of sterile packages
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEEDLEMASTER 4MMx 25G LOWER
The Issue: Inspection confirmed a small percentage of sterile packages
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX UP 2MM CH 25G 5MM
The Issue: Inspection confirmed a small percentage of sterile packages
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KD-640L ELECTROSURGICAL SNARE
The Issue: Inspection confirmed a small percentage of sterile packages
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KD-650U ELECTROSURGICAL SNARE
The Issue: Inspection confirmed a small percentage of sterile packages
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEEDLEMASTER 4MMx 25G UPPER
The Issue: Inspection confirmed a small percentage of sterile packages
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEEDLEMASTER 4MMx 21G UPPER
The Issue: Inspection confirmed a small percentage of sterile packages
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX UP 2MM CH 25G 6MM
The Issue: Inspection confirmed a small percentage of sterile packages
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KD-612U ELECTROSURGICAL SNARE
The Issue: Inspection confirmed a small percentage of sterile packages
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.