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 14621–14640 of 38,428 recalls
Recalled Item: NanoClave Stopcock w/NanoClave
The Issue: Identification of a potential manufacturing defect on the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11" (28 cm) Appx 1.7 ml
The Issue: Identification of a potential manufacturing defect on the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.5" (14 cm) Appx 0.28 ml
The Issue: Identification of a potential manufacturing defect on the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6 IN (15cm) APPX 0.89ml
The Issue: Identification of a potential manufacturing defect on the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6 IN (15 cm) Ext Set
The Issue: Identification of a potential manufacturing defect on the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8.5" (22 cm) Appx 0.57 ml
The Issue: Identification of a potential manufacturing defect on the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" (18 cm) Appx 0.29 ml
The Issue: Identification of a potential manufacturing defect on the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10" (25 cm) Appx 2.8 ml
The Issue: Identification of a potential manufacturing defect on the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 22" (56 cm) Appx 2.5 ml
The Issue: Identification of a potential manufacturing defect on the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 15 cm (6 IN) Appx 1.1 ml
The Issue: Identification of a potential manufacturing defect on the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9.5" (24 cm) Appx 0.56 ml
The Issue: Identification of a potential manufacturing defect on the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 60 IN (152cm) APPX 1.1ml
The Issue: Identification of a potential manufacturing defect on the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 126 IN (320cm) APPX 23.5ml
The Issue: Identification of a potential manufacturing defect on the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" (18 cm) Appx 0.31 ml
The Issue: Identification of a potential manufacturing defect on the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" (18 cm) Appx 0.25 ml
The Issue: Identification of a potential manufacturing defect on the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20 cm (8 IN) APPX 1.0ml
The Issue: Identification of a potential manufacturing defect on the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 149 IN (378cm) APPX 19.1 ml
The Issue: Identification of a potential manufacturing defect on the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 40 (102cm) Appx 4.4ml Ext Set
The Issue: Identification of a potential manufacturing defect on the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7 IN(18 cm)APPX 1.2ml. EXT SET
The Issue: Identification of a potential manufacturing defect on the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 58 IN (147cm) APPX 8.0 ml
The Issue: Identification of a potential manufacturing defect on the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.