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 Numbers; 102151, 103108, 103218, K132627, K148054, K156266, K163449, K176543, K197127, K211492, K535999, K555552, K586403, K626840, K667012, K678478, K705482
  • Product Classification
    Anesthesiology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    4902 Glass L.O.R. Syringe
  • Manufacturer
    Smiths Medical ASD, Inc.
Device Recall Portex
  • Model / Serial
    Lot Numbers: 102517, K154089, K211495, K222113, K512485, K522220, K538711, K559480, K573554, K618300, K643592, K669735, K686834, K700785
  • Product Classification
    Anesthesiology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    4903 Glass L.O.R. Syringe
  • Manufacturer
    Smiths Medical ASD, Inc.
Device Recall Portex
  • Model / Serial
    Lot Numbers: 102518, K163468, K176555, K510385, K520203, K529939, K532723, K533729, K586882, K633942, K675421, K676747, K681955, K682698
  • Product Classification
    Anesthesiology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    4904 Glass L.O.R. Syringe
  • Manufacturer
    Smiths Medical ASD, Inc.
Device Recall Portex
  • Model / Serial
    Lot Numbers: 101219, 103102, 105025, 106337, 109045, 110699, 111198, K110057, K110924, K124484, K128817, K132629, K141382, K144904, K147200, K148053, K157883, K160686, K163440, K189808, K211510, K221874, K511628 4950-17
  • Product Classification
    Anesthesiology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    4950-16 Portex¿ Epidural Mini-pack
  • Manufacturer
    Smiths Medical ASD, Inc.
Device Recall Portex
  • Model / Serial
    Lot Numbes: 101146, 101452, 105024, 107076, 109224, 111199, K110058, K121072, K124485, K128818, K132630, K141613, K143220, K147085, K151519, K163451, K180107, K189821, K211507, K223552, K527934, K541698, K558498, K598204, K632932, K638749, K642968, K656458, K699000
  • Product Classification
    Anesthesiology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide
  • Product Description
    4950-17 Portex¿ Epidural Mini-pack
  • Manufacturer
    Smiths Medical ASD, Inc.
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