Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 2,029–2,040 of 2,908 recalls
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
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
Potential for early life x-ray tube failure for mobile x-ray system due to excessive thermal load on the anode.
Potential for early life x-ray tube failure for mobile x-ray system due to excessive thermal load on the anode.
Incorrect resistor utilized in the VH-3010 Power Supply, which may cause the jaws of the HemoPro 2 to not adequately heat up.
the impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.
the impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.
the impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.