Devices

Device Recall Portex

Manufacturer

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

117 devices with a similar name

Learn more about the data here

Device Recall Portex
  • Model / Serial
    Lot Number: K521793
  • Product Classification
    Anesthesiology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    15711-20 SPINAL(DD) 27G QUINCKE W/DRUGS
  • Manufacturer
    Smiths Medical ASD, Inc.
Device Recall Portex
Device Recall Portex
  • Model / Serial
    Lot Number: K516849
  • Product Classification
    Anesthesiology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    15249-21 SPINAL(DD) 22/25G QUINCKE W/DRUGS
  • Manufacturer
    Smiths Medical ASD, Inc.
Device Recall Portex
  • Model / Serial
    Lot Number: K515994
  • Product Classification
    Anesthesiology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    15524-20 SPINAL(DD) 22G QUINCKE 25G DIAMOND POINT W/DRUGS
  • Manufacturer
    Smiths Medical ASD, Inc.
Device Recall Portex
  • Model / Serial
    Lot Numbers: K514753, K515420, K519328
  • Product Classification
    Anesthesiology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    15545-20 SPINAL(DD) 25G W/DRUGS
  • Manufacturer
    Smiths Medical ASD, Inc.
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