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 24201–24220 of 38,428 recalls
Recalled Item: PE CONNECTOR 3/8 Y 20/BX
The Issue: Labeling: The expiration date is not stated on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Hemaduct Cardiothoracic Silicone Round Drain
The Issue: Product's seal possibly compromised, potentially compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Hemaduct Silicone Round Drain
The Issue: Product's seal possibly compromised, potentially compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Hemaduct Silicone Round Drain
The Issue: Product's seal possibly compromised, potentially compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Silicone Round Drain
The Issue: Product's seal possibly compromised, potentially compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PE CONNECTOR 3/8 STRAIGHT 20/BX
The Issue: Labeling: The expiration date is not stated on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Hemaduct Silicone Round Drain
The Issue: Product's seal possibly compromised, potentially compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Hemaduct Silicone Flat Drain
The Issue: Product's seal possibly compromised, potentially compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Silicone Flat Drain
The Issue: Product's seal possibly compromised, potentially compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Hemaduct Silicone Round Drain
The Issue: Product's seal possibly compromised, potentially compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Silicone Flat Drain
The Issue: Product's seal possibly compromised, potentially compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFANT 20/BX Recalled by Teleflex Medical Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Hemaduct Silicone Round Drain
The Issue: Product's seal possibly compromised, potentially compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Silicone Flat Drain
The Issue: Product's seal possibly compromised, potentially compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N265)
The Issue: The integrity of the product container may be
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Streptococcus Susceptibility card (AST-ST01)
The Issue: The integrity of the product container may be
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Fungal Susceptibility card (AST-YS08)
The Issue: The integrity of the product container may be
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Positive Susceptibility card (AST-GP67)
The Issue: The integrity of the product container may be
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N340)
The Issue: The integrity of the product container may be
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-GN76)
The Issue: The integrity of the product container may be
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.