Devices

STRETCHER

  • Modelo / Serial
    Model Catalog: 1005-000-000 (Lot serial: beginning with 0407 to 0701); Model Catalog: 1009-000-000 (Lot serial: beginning with 0407 to 0701); Model Catalog: 1001-000-000 (Lot serial: beginning with 0407 to 0701); Model Catalog: 0735-000-000 (Lot serial: beginning with 0407 to 0701); Model Catalog: 0721-000-000 (Lot serial: beginning with 0407 to 0701); Model Catalog: 0660-000-000 (Lot serial: beginning with 0407 to 0701); Model Catalog: 1731-000-000 (Lot serial: beginning with 0309 to 0505); Model Catalog: 1710-000-000 (Lot serial: beginning with 0309 to 0505); Model Catalog: 1509-000-000 (Lot serial: beginning with 0309 to 0505); Model Catalog: 1501-000-000 (Lot serial: beginning with 0309 to 0505); Model Catalog: 1231-000-000 (Lot serial: beginning with 0309 to 0505); Model Catalog: 1210-000-000 (Lot serial: beginning with 0309 to 0505); Model Catalog: 1069-000-000 (Lot serial: beginning with 0309 to 0505); Model Catalog: 1025-000-000 (Lot serial: beginning with 0309 to 0505); Model Catalog: 1020-000-000 (
  • Descripción del producto
    STRETCHERS
  • Manufacturer
    STRYKER CANADA LP
  • 1 Event

Fabricante

STRYKER CANADA LP
  • Dirección del fabricante
    HAMILTON
  • Empresa matriz del fabricante (2017)
    Stryker
  • Source
    HC

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Device Recall Ferno Model 35X PROFlexx Stretchers
  • Modelo / Serial
    The following serial numbers are affected by this recall: 13N272700 13N273357 13N273915 13N274967 13N275720 13N272701 13N273358 13N273916 13N274968 13N275721 13N272702 13N273359 13N273917 13N274969 13N275722 13N272703 13N273360 13N274387 13N274970 13N275723 13N272704 13N273361 13N274388 13N274971 13N275724 13N272705 13N273362 13N274389 13N274972 13N275725 13N273353 13N273363 13N274390 13N274973 13N275726 13N273354 13N273902 13N274391 13N275717 13N273355 13N273913 13N274965 13N275718 13N273356 13N273914 13N274966 13N275719
  • Clasificación del producto
    General Hospital and Personal Use Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    The affected product was distributed to the following states: OH, MA, HI, NJ, TN, TX, MO, and GA. The affected product was distributed to the following foreign countries: Canada, Germany and Venezuela.
  • Descripción del producto
    Ferno Model 35X PROFlexx Stretchers, one unit per package
  • Manufacturer
    Ferno-Washington Inc
Device Recall Sechrist Low Profile Wheeled Stretcher
  • Modelo / Serial
    Lot Code: 0086 0088 0024 0054 0056 0031 0040 0085 0046 0051 0121 0042 0032 0036 0021 0022 0015 0020 0065 0074 0066 0069 0007 0017 0005 0018 0004 0008 0062 0063 0038 0043 0033 0035 0037 0058 0071 0010 0011 0019 0049 0050 0055 0023 0039 0045 0059 0064 0028 0041 0044 0025 0001 0014 0068 0073 0057 0060 0027 0029 0030 0082 0083 0048 0070 0072 0034 0047 0009 0013 0080 0002 0081 0090 0091   Item No. 21762-135-33HJ 21762-135-33HJ 21762-135-33HJ 21762-135-33HJ 21762-135-33HJ 21762-110-36H
  • Clasificación del producto
    General Hospital and Personal Use Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    US Distribution and Internationally to Japan and Jordan.
  • Descripción del producto
    Sechrist Low Profile Wheeled Stretcher, Model No. 21762-110-33H, 21762-110-36H, 21762-110-41H, 21762-135-33HJ, 21762-010-36H, 21762-010-41H, || 21762-111-36H.
  • Manufacturer
    Sechrist Industries Inc
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