Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 481–492 of 607 recalls
Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
Discrepancies between sterilization instructions in the Japanese language product package inserts and those published in the manufacturer product Instructions For Use (IFU).
Ultrasound transducer devices were refurbished beyond their useful life.
Ultrasound transducer devices were refurbished beyond their useful life.
Ultrasound transducer devices were refurbished beyond their useful life.
Ultrasound transducer devices were refurbished beyond their useful life.
Ultrasound transducer devices were refurbished beyond their useful life.
Ultrasound transducer devices were refurbished beyond their useful life.
Ultrasound transducer devices were refurbished beyond their useful life.
Ultrasound transducer devices were refurbished beyond their useful life.