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 33641–33660 of 38,428 recalls
Recalled Item: Weck Vista Universal Laparoscopic Port
The Issue: Complaints of leakage of insufflation gas through the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 mm Weck Vista Universal Cannula
The Issue: Complaints of leakage of insufflation gas through the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 Weck Vista Universal Balloon Open Access Port - Standard Length (70mm)
The Issue: Complaints of leakage of insufflation gas through the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures
The Issue: The products are being recalled because they did
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12 mm Weck¿ Vista" Optical Bladeless Laparoscopic Access Port
The Issue: Complaints were received of leakage of insufflation gas
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 mm Weck¿
The Issue: Complaints were received of leakage of insufflation gas
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures
The Issue: The products are being recalled because they did
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weck¿ Vista"
The Issue: Complaints were received of leakage of insufflation gas
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weck¿ Vista" Universal Laparoscopic Port
The Issue: Complaints were received of leakage of insufflation gas
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 Weck¿ Vista" Universal Balloon Open Access Port - Long Length (100mm)
The Issue: Complaints were received of leakage of insufflation gas
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10mm Weck¿ Vista" Cannula-only
The Issue: Complaints were received of leakage of insufflation gas
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 Weck¿ Vista" Universal Balloon Open Access Port Short Length (53mm)
The Issue: Complaints were received of leakage of insufflation gas
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12 Weck¿ Vista" Universal Balloon Open Access Port Long Length (100mm)
The Issue: Complaints were received of leakage of insufflation gas
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12mm Weck¿ Vista" Cannula-only
The Issue: Complaints were received of leakage of insufflation gas
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12MM X 100MM Weck¿ Vista" UNIVERSAL CONE OPEN ACCESS
The Issue: Complaints were received of leakage of insufflation gas
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weck¿ Vista" Universal Laparoscopic Port
The Issue: Complaints were received of leakage of insufflation gas
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures
The Issue: The products are being recalled because they did
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Suture
The Issue: The products are being recalled because they did
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12 Weck¿ Vista" Universal Balloon Open Access Port Standard Length (70mm)
The Issue: Complaints were received of leakage of insufflation gas
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 mm Weck¿
The Issue: Complaints were received of leakage of insufflation gas
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.