Devices

Device Recall 0.9 Sodium Chloride Injection, USP

  • Modèle / numéro de série
    KH04143,exp. 07/2016; KH04145, exp. 08/2016; KH04153, exp. 11/2016; KH04155, exp. 12/2016
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Distributed in the states of CA. PA, VA, TX, MA, MD, WV, UT, FL, and TN.
  • Description du dispositif
    0.9% Sodium Chloride Injection, USP, 10mL in 12mL., Single use, Rx only, Sterile Solution.
  • Manufacturer
    MRP, LLC dba AMUSA
  • 1 Event

Fabricant

MRP, LLC dba AMUSA
  • Adresse du fabricant
    MRP, LLC dba AMUSA, 5209 Linbar Dr Ste 640, Nashville TN 37211-1026
  • Société-mère du fabricant (2017)
    Amusa Inc.
  • Source
    USFDA