Device Recall CLINITRON CII

  • Model / Serial
    Model CII, Serial #CC(all numeric codes).
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    The units are primarily leased to hospitals. Units have been sold to hospitals located nationwide and to Canada, Austria, France, Germany Ireland Italy, Netherlands, Spain, Sweden, Switzerland and the United Kingdom.
  • Product Description
    CLINITRON CII Air Fluidized Therapy unit.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Hill-Rom Manufacturing, Inc., 4349 Corporate Road, Charleston SC 29405
  • Source
    USFDA

One device with a similar name

Learn more about the data here

  • Model / Serial
    All serial numbers.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution -- United States, Abu Dhabi, Brazil, Canada, Chile, Columbia, Mexico, Newfoundland, Puerto Rico, Saudi Arabia, Singapore, Taiwan, Turkey and Venezuela.
  • Product Description
    CLINITRON¿ CII Air Fluidized Therapy Units. || Intended to prevent and/or treat pressure ulcer development and wound deterioration in patients who have a significant risk of developing these problems and who generally also have one or more of the following conditions: immobility, poor nutrition, diminished level of consciousness, reduced subcutaneous tissue or multi-system failure.
  • Manufacturer