Recall Z-1603-2008

Hill-Rom, Inc. · initiated April 8, 2008

Terminated

Product

Hill-Rom 100 Low Bed; Model No. P3930.

Codes / lots: All units.

Reason for recall

The upper deck may collapse to its lowest position and the caster brakes may fracture if the bed is moved while the brakes are locked.

FDA-determined cause: Device Design

Action taken

Consignees were notified via letter dated April 8, 2008 to lower these beds to their lowest position, to remove the beds from use if they move more than 1/2 inch with the brakes locked and that the firm will repair these beds when fixes become available. If you have questions regarding this recall, contact Hill-Rom Technical Support at 800-445-3730.

Details

Recall number
Z-1603-2008
Initiated
April 8, 2008
Posted by FDA
September 5, 2008
Terminated
October 13, 2010
Product code
FNL – Bed, Ac-Powered Adjustable Hospital
Quantity
753 beds
Distribution
Worldwide: USA and Canada.
Recalling firm
Hill-Rom, Inc., Batesville, IN

Official FDA recall record