Devices

Device Recall Portex

  • Modelo / 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
  • Clasificación del producto
    Anesthesiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide
  • Descripción del producto
    4950-17 Portex¿ Epidural Mini-pack
  • Manufacturer
    Smiths Medical ASD, Inc.
  • 1 Event

Fabricante

Smiths Medical ASD, Inc.
  • Dirección del fabricante
    Smiths Medical ASD, Inc., 10 Bowman Dr, Keene NH 03431-5043
  • Empresa matriz del fabricante (2017)
    Smiths Group Plc
  • Source
    USFDA

117 dispositivos con un nombre similar

Más información acerca de la data acá

Device Recall Portex
  • Modelo / Serial
    Part Number 384001, 20 per case, Lot numbers: 551880804, 581451104, 581461104;  Part Number 386000, 15 per case, Lot numbers: 551890804, 600080205, 5518908004
  • Clasificación del producto
    Anesthesiology Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Product was distributed domestically to customers in CA, AZ, IL, CO, OR, FL, VA, OH, MI, and UT. Product was also distributed to the following foreign countries: Malaysia, Mexico, and New Zealand
  • Descripción del producto
    Portex Adult Single Limb Anesthesia Breathing Circuit, single use, Part Numbers: 386000 and 384001. Manufactured for Sims Portex, Inc., Fort Meyers, FL, Made in Mexico.
  • Manufacturer
    MMS Sales Corp
Device Recall Portex
Device Recall Portex
Device Recall Portex
  • Modelo / Serial
    Lot Numbers; 102151, 103108, 103218, K132627, K148054, K156266, K163449, K176543, K197127, K211492, K535999, K555552, K586403, K626840, K667012, K678478, K705482
  • Clasificación del producto
    Anesthesiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide
  • Descripción del producto
    4902 Glass L.O.R. Syringe
  • Manufacturer
    Smiths Medical ASD, Inc.
Device Recall Portex
  • Modelo / Serial
    Lot Numbers: 102517, K154089, K211495, K222113, K512485, K522220, K538711, K559480, K573554, K618300, K643592, K669735, K686834, K700785
  • Clasificación del producto
    Anesthesiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide
  • Descripción del producto
    4903 Glass L.O.R. Syringe
  • Manufacturer
    Smiths Medical ASD, Inc.
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