Device Recall BLUE BURN SHEET

  • Model / Serial
    Lot Numbers: JT13607, JT17507, JT35207, JT09008, JT11308, JT15408, JT18408, JT18708, JT23408, JT24508, JT26408, JT28408, JT31408, JT33508, JT00609, JT04809, JT15209, JT18209, JT19209, JT22409, JT22709, JT23209, JT25309, JT25809, JT27509, JT30109, JT31309, JT32909, JT17510, JT23610, JT24010, JT24810, JT30810, JT35910, JT00811, JT05011, JT07911, JT11511, JT15911, JT17011, JT18211, JT21511, JT26311, JT28411, JT30711, JT00812, JT07312, JT11812, JT13612, JT17712, JT21812, JT25612, JT33012, JT36112, JT36212, JT09113, JT17513, JT24713, JT29813, JT33513, JT01614, JT04614, JT06814
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Worldwide distribution - US Nationwide in the states of: CA, CO, CT, FL, GA, IL, CO, NY, NV, IN, MD, MO, MD OH, TN, TX & WI; and country of Canada
  • Product Description
    BLUE BURN SHEET, STERILE, 60" x 96"; Item 7305, GAM item 30-01 || Product Usage - May provide a sterile, barrier environment to protect patient from infection.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Dukal Corp., 2 Fleetwood Ct, Ronkonkoma NY 11779-6907
  • Manufacturer Parent Company (2017)
  • Source
    USFDA