Devices

Device Recall Safety Laceration Kit

  • Modèle / numéro de série
    Model number: 59108B, Lot number: 187210, Exp. Date: 2/1/2017.
  • Classification du dispositif
    General and Plastic Surgery Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Distributed in the states of AR, AZ, FL, GA, IA, IL, KY, MA, MN, NC, NY, OH, TN, TX, and VA.
  • Description du dispositif
    Safety Laceration Kit, Sterile Single Use, Latex Free, 20/case, Medical Action Industries, Inc, Arden, NC.
  • Manufacturer
    Medical Action Industries Inc
  • 1 Event

Fabricant

Medical Action Industries Inc
  • Adresse du fabricant
    Medical Action Industries Inc, 25 Heywood Rd, Arden NC 28704-9302
  • Société-mère du fabricant (2017)
    Owens & Minor Inc
  • Source
    USFDA