Devices

Device Recall ULTRA Fabric Reinforced Surgical Gown

  • Modèle / numéro de série
    Product Code: 95221-35, Unit Code: 90372
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    US (nationwide) including the states of CA, CO, LA, NM, OK, TX and WA.
  • Description du dispositif
    ULTRA Fabric Reinforced Surgical Gown, X-Large, Sterile, Test File. || The Kimberly-Clark ULTRA Fabric Reinforced Surgical Gown is a sterile, single use surgical gown intended to protect surgical patients and operating room personnel from the transfer of microorganisms, body fluids, and particulate material.
  • Manufacturer
    Kimberly-Clark Corporation
  • 1 Event

Fabricant

Kimberly-Clark Corporation
  • Adresse du fabricant
    Kimberly-Clark Corporation, 1400 Holcomb Bridge Rd, Roswell GA 30076
  • Source
    USFDA

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Device Recall ULTRA Fabric Reinforced surgical Gown XLarge Sterile
  • Modèle / numéro de série
    Product Code 95221 - All lot numbers beginning with: AH9284*** to AH9356***, AH0007*** to AH0356***, AH1008 *** to AH1364***, AH2006*** to AH2146***
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution
  • Description du dispositif
    ULTRA Fabric Reinforced surgical Gown X-Large Sterile || The product is a sterile, single use, surgical gown intended to protect surgical patients and operating room personnel from the transfer of microorganisms, body fluids, and particulate material.
  • Manufacturer
    Kimberly-Clark Corporation