Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 397–408 of 3,866 recalls
Software issue: When programming the SynchroMed Pump with the A810 CP App in Flex Infusion Mode, the infusion steps should automatically be arranged in consecutive order, from earliest to latest.…
Stent-assisted coiling device may due to commingling during manufacturing have dimensional nonconformance and/or incorrect device configuration.…
Incomplete seals on sterile product
Incomplete seals on sterile product
Incomplete seals on sterile product
Incomplete seals on sterile product
Incomplete seals on sterile product
Incomplete seals on sterile product
Incomplete seals on sterile product
Incomplete seals on sterile product
Incomplete seals on sterile product
Incomplete seals on sterile product