Devices

Device Recall Epidural Needle

  • Modèle / numéro de série
    Lot No. RF4044686, expiration date 2006-09
  • Classification du dispositif
    Anesthesiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    The recalled kits with the wrong epidural needle was distributed to the following direct accounts, to the following states in TN and TX
  • Description du dispositif
    ARROW EPIDURAL CATHETERIZATION KIT. Product No. MC-05001.
  • Manufacturer
    Arrow International Inc
  • 1 Event

Fabricant

Arrow International Inc
  • Adresse du fabricant
    Arrow International Inc, 2400 Bernville Rd, Reading PA 19605-9607
  • Société-mère du fabricant (2017)
    Teleflex Incorporated
  • Source
    USFDA