Device Recall OPHTHALMIC DRS 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: 2016081550 4/30/19 2016080950 4/30/19 2016072250 12/31/18 2016051350 10/31/18 2016030550 4/30/18 2016022350 4/30/18 2016011850 4/30/18 2015122150 4/30/18 2015121450 4/30/18 2015101250 4/30/18 2015070750 2/28/18 2015062950 2/28/18 2015061950 1/31/18 2015062250 2/28/18 2015051850 1/31/18 2015050450 2/28/18 2015042850 11/30/17 2015031950 11/30/17 2015010750 10/31/17 2014103150 7/31/17 2014102750 7/31/17 2014073050 5/31/17
  • 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
    OPHTHALMIC DRS 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