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: K519326
  • Product Classification
    Anesthesiology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    4804-20 SPINAL(DD) 22G WHITACRE W/DRUGS
  • Manufacturer
    Smiths Medical ASD, Inc.
Device Recall Portex
  • Model / Serial
    Lot Number: K517129
  • Product Classification
    Anesthesiology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    49651-22 SPINAL 22G PENCIL POINT W/DRUGS
  • Manufacturer
    Smiths Medical ASD, Inc.
Device Recall Portex
  • Model / Serial
    Lot Numbers: K534360, K547115, K671715, K687779
  • Product Classification
    Anesthesiology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    A3176-18 Portex¿ Epidural Mini-pack
  • Manufacturer
    Smiths Medical ASD, Inc.
Device Recall Portex
  • Model / Serial
    Lot Number: K518190
  • Product Classification
    Anesthesiology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    49651-24 SPINAL 24G EUROPEAN PENCIL POINT W/DRUGS
  • Manufacturer
    Smiths Medical ASD, Inc.
Device Recall Portex
  • Model / Serial
    Lot Numbers: K515853, K517107, K518986, K522227
  • Product Classification
    Anesthesiology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    49651-25 SPINAL 25G PENCIL POINT W/DRUGS
  • Manufacturer
    Smiths Medical ASD, Inc.
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