Recall Z-0088-2009
Hill-Rom Manufacturing, Inc. · initiated June 19, 2008
Product
Envision E700 Low Airloss Therapy Surface, Made By Hill-Rom Manufacturing, Inc., Charleston, SC. The Envision E700 Low Airloss Therapy Surface helps prevent and treat stage III and stage IV pressure ulcers in patients who weigh between 70 lb and 400 lb and are between 4'11" and 6' 4" in height.
Codes / lots: Serial numbers DB100527 thru DB101305.
Reason for recall
A defect in the software of the device may not allow the patient bed exam alarm or the patient movement alarm to function correctly.
FDA-determined cause: Software change control
Action taken
An internal Modification Notice dated 9/1/08 was sent via email to Service Centers (because the device is owned by the manufacturer, Hill-Rom, each Service Center in possession of the device will be the consignee). Each Service Center will perform the correction on the units affected. Each device in the affected serial number range will be tested for the software defect. If the defect is found, the circuit board that contains the defective software will be replaced. The Field Action Plan is expected to be completed on July 24, 2008. Expected completion date of the Correction will be 12 months from July, 2008.
Details
- Recall number
- Z-0088-2009
- Initiated
- June 19, 2008
- Posted by FDA
- October 7, 2008
- Terminated
- May 21, 2009
- Product code
- IOQ – Bed, Flotation Therapy, Powered
- Quantity
- 779 units
- Distribution
- Worldwide Distribution --- including USA and country of Canada.
- Recalling firm
- Hill-Rom Manufacturing, Inc., Charleston, SC