Device Recall Portex

  • Model / Serial
    Lot Numbes: 101146, 101452, 105024, 107076, 109224, 111199, K110058, K121072, K124485, K128818, K132630, K141613, K143220, K147085, K151519, K163451, K180107, K189821, K211507, K223552, K527934, K541698, K558498, K598204, K632932, K638749, K642968, K656458, K699000
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    4950-17 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