Device Recall Portex

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 Number: K516574
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    15816-21 SPINAL(DD) 27G QUINCKE W/DRUGS
  • Manufacturer
  • Model / Serial
    Lot Number: K516550
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    15830-21 SPINAL(DD) 25G WHITACRE W/DRUGS
  • Manufacturer
  • Model / Serial
    Lot Number: K521691
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    15848-20 SPINAL(DD) 24G SPROTTE W/DRUGS
  • Manufacturer
  • Model / Serial
    Lot Number: K516575
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    15955-21 SPINAL(DD) 25G WHITACRE W/DRUGS
  • Manufacturer
  • Model / Serial
    Lot Number: 2782094
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    US in the state of FL.
  • Product Description
    Portex Anaerobic Pulsator Arterial Blood Sampling Kit, with Liquid Sodium Heparin for Gases and Electrolytes. || Reorder Number: G1392 || Product Usage: The Arterial Blood Sampling Kit is intended for sampling arterial blood for the measurement of blood gasses, Cooximetry, electrolytes, total magnesium, and metabolites, (Glucose and Lactate).
  • Manufacturer
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