Device Recall AMO Prestige Pack

  • Model / Serial
    Lot # Exp. date 3JR190 10/2006 3KR128 11/2006 3LR100 12/2006 3MR002 12/2006 3MR047 12/2006 3MR048 12/2006 3MR081 01/2007 3MR082 01/2007 4AR045 01/2007 4AR050 01/2007 4AR058 01/2007
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Distribution was to 67 domestic customers and internationally.
  • Product Description
    Surgical Tubing Pack, Model: AMO Prestige Pack, Product Code OPO40
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Allergan Medical Optics Inc, 1700 E Saint Andrew Pl, Santa Ana CA 92705-4933
  • Source
    USFDA