Devices

Device Recall Epidural Needle

  • Modelo / Serial
    Lot No. RF4044686, expiration date 2006-09
  • Clasificación del producto
    Anesthesiology Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    The recalled kits with the wrong epidural needle was distributed to the following direct accounts, to the following states in TN and TX
  • Descripción del producto
    ARROW EPIDURAL CATHETERIZATION KIT. Product No. MC-05001.
  • Manufacturer
    Arrow International Inc
  • 1 Event

Fabricante

Arrow International Inc
  • Dirección del fabricante
    Arrow International Inc, 2400 Bernville Rd, Reading PA 19605-9607
  • Empresa matriz del fabricante (2017)
    Teleflex Incorporated
  • Source
    USFDA