Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 973–984 of 4,586 recalls
Potential for the balloon in the device to not meet burst specifications.
A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an incorrect thread.
A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an incorrect thread.
Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments
Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments
Due to increased complaints for broken/frayed grip cables for reusable instruments.
Due to increased complaints for broken/frayed grip cables for reusable instruments.
Due to increased complaints for broken/frayed grip cables for reusable instruments.
Due to increased complaints for broken/frayed grip cables for reusable instruments.
Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the system to become inoperable.…
Following a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the system to become inoperable.…
There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.