Atlas FDA

Medtronic

10 FDA 510(k) clearances · Recalling firm

Sort:Newest firstOldest first

◉ Watch Medtronic

RecordFirmDate
BNX Fine Need Aspiration System (19GA); Material/Part #: DSN-19-01 recall (Z-1472-2017)Medtronic2017-02-28
SharkCore Fine Needle Biopsy System (22 GA); Material/Part #s: DSC-22-01 recall (Z-1473-2017)Medtronic2017-02-28
SharkCore Fine Needle Biopsy System (25GA); Material/Part#: DSC-25-01 recall (Z-1474-2017)Medtronic2017-02-28
SharkCore LG Fine Needle Biopsy System (19GA); Material/Part#: DSL-19-01 recall (Z-1475-2017)Medtronic2017-02-28
BNX Fine Need Aspiration System (22GA); Material/Part#: DSN-22-01 recall (Z-1476-2017)Medtronic2017-02-28
Battery Pack Used with the Capnostream"20 and Capnostream"20p Patient Monitor, Battery Pac recall (Z-1577-2016)Medtronic2016-05-12
Covidien Endo GIA Ultra Universal 12 mm Short Stapler Handle Ref: EGIAUSHORT Product Usage recall (Z-0819-2016)Medtronic2016-02-18
Covidien Endo GIA Ultra Universal Standard Stapler Handle Ref: EGIAUSTND Product Usage: Th recall (Z-0820-2016)Medtronic2016-02-18
Covidien Endo GIA Ultra Universal 12 mm XL Stapler Handle Ref: EGIAUXL Product Usage: The recall (Z-0821-2016)Medtronic2016-02-18
Best Practice Kits containing certain production lots of Endo GIA Ultra Universal Stapler recall (Z-0822-2016)Medtronic2016-02-18

Track Medtronic automatically

Every clearance here is in the API, with alerts when new ones post.