Devices

Device Recall Re Turn

  • Modèle / numéro de série
    All affected product in the U.S are from the same LOT #1402S, Model #s 6133-6136
  • Classification du dispositif
    Physical Medicine Devices
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    US Distribution to the states of : FL, CA, NJ, NC and MD.
  • Description du dispositif
    ReTurn belt, wipeable, sizes Small through Extra Large, Plastic pouch, 1 item per pouch. Patient transfer aid.
  • Manufacturer
    Handicare USA, Inc.
  • 1 Event

Fabricant

Handicare USA, Inc.
  • Adresse du fabricant
    Handicare USA, Inc., 2201 Hangar Pl, Ste 200, Allentown PA 18109-9342
  • Société-mère du fabricant (2017)
    Handicare Group Ab
  • Source
    USFDA