Device Recall Portex

  • Model / Serial
    Lot Numbers: 102518, K163468, K176555, K510385, K520203, K529939, K532723, K533729, K586882, K633942, K675421, K676747, K681955, K682698
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    4904 Glass L.O.R. Syringe
  • 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
    All Lot Numbers
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    Portex Inner Cannula for Tracheostomy Tube, 8.0 mm, REF Code 566080
  • Manufacturer
  • Model / Serial
    Lot Number: K521049
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    Smiths Medical ASD, Inc. Regional Anesthesia Trays containing the Hospira 2ml drug ampuls of 5% Lidocaine Hydrochloride with 7.5% Dextrose Injection, (NDC 0074-4712-01, lot number 09-568-DK) as follows: || Product Number/Description || 15248C-22/25 SPINAL TRAY 22/25 (SDD)W/DRUGS
  • Manufacturer
  • Model / Serial
    Lot Number: K521793
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    15711-20 SPINAL(DD) 27G QUINCKE W/DRUGS
  • Manufacturer
  • Model / Serial
    Lot Number: K516849
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    15249-21 SPINAL(DD) 22/25G QUINCKE W/DRUGS
  • Manufacturer
112 more