Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 913–924 of 1,121 recalls
Due to evaporator gasket not sealing which can cause liquid nitrous oxide to drip/leak from the bottom of the device handle during treatment or after treatment during venting of the device
Incorrect resistor utilized in the VH-3010 Power Supply, which may cause the jaws of the HemoPro 2 to not adequately heat up.
The battery for certain ultrasound systems can potentially develop an internal failure which could result in smoke or fire.
The battery for certain ultrasound systems can potentially develop an internal failure which could result in smoke or fire.
Potential for collimator to fall as a result of incorrect installation.
Potential for collimator to fall as a result of incorrect installation.
Lack of sterility assurance for closed suction catheter systems
Lack of sterility assurance for closed suction catheter systems
Lack of sterility assurance for closed suction catheter systems
Lack of sterility assurance for closed suction catheter systems
Lack of sterility assurance for closed suction catheter systems
Lack of sterility assurance for closed suction catheter systems