The firm manufactured and distributed custom surgical kits which contained BD SafetyGlide" 22GA 1¿ inch Needles. BD subsequently recalled these needles because, " Loose polypropylene particulate in the fluid path could be expelled out of the needle during injection.
Surgical Instruments
🏥 Medical Devices • 6,839 recalls
Punctures in blister packaging that was detected during the packaging process.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Insufficient documentation to support product sterility claims.
Devices are not consistent with Quality System Requirements.
Insufficient documentation to support product sterility claims.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Insufficient documentation to support product sterility claims.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.