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: K221961
  • Product Classification
    Anesthesiology Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    CA, CO, FL, GA, IN, MA, MD, MI. NH, NC, NY, TX, WA
  • Product Description
    Portex Tracheal Tube Guide 15 Fr, non-sterile || Catalog Number: 153013
  • Manufacturer
    Smiths Medical ASD, Inc
Device Recall Portex/Sims Portex
  • Model / Serial
    All Lot Numbers
  • Product Classification
    Anesthesiology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    Portex Inner Cannula for Tracheostomy Tube, 8.0 mm, REF Code 566080
  • Manufacturer
    Smiths Medical ASD, Inc
Device Recall Portex
  • Model / Serial
    Lot Number: K521049
  • Product Classification
    Anesthesiology Devices
  • 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
    Smiths Medical ASD, Inc.
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
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