Device Recall Portex

  • Model / Serial
    Lot Numbers: K167341, K184428, K197145, K209523, K222123, K502514, K512986, K517133, K523565, K525700, K529957, K554390, K558495, K573614, K630925, K633623, K656459, K673351, K688226, K704809
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    4954-17 Portex¿ Epidural Mini-pack
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Smiths Medical ASD, Inc., 10 Bowman Dr, Keene NH 03431-5043
  • Manufacturer Parent Company (2017)
  • Source
    USFDA

117 devices with a similar name

Learn more about the data here

  • Model / Serial
    Lot Numbers: K516347, K520553, K522055
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    A2526-24 SPINAL (SHB) W/DRUGS
  • Manufacturer
  • Model / Serial
    Lot Numbers: K515876, K520197, K522302
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    A2613 SPINAL(FL)W/DRUGS
  • Manufacturer
112 more