Device Recall POSTOP EYE TRAY

  • Modèle / numéro de série
    Centurion component code 2841, Affected product was placed into Centurion Convenience Kits between July 2013 and January 2017. Batch Numbers & Exp. dates: 2016100390 12/31/18 2016092190 12/31/18 2016072790 10/31/18 2016061590 4/30/18 2016031490 4/30/18 2016022390 4/30/18 2015111190 4/30/18 2015092890 4/30/18 2015083190 9/30/17 2015032390 10/31/17 2015052890 9/30/17 2015052090 9/30/17 2015050590 9/30/17
  • Classification du dispositif
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    US Distribution: NY, NC, PA, CA, OH, WA, VA, NJ, IL
  • Description du dispositif
    POST-OP EYE TRAY || The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into non-sterile Centurion Convenience Kits along with other || components.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Centurion Medical Products Corporation, 100 Centurion Way, Williamston MI 48895-9086
  • Société-mère du fabricant (2017)
  • Source
    USFDA