RecallDepth

Hill-Rom Procedural Stretcher with auto-contour option; Model P8000F. Wheeled hospital stretcher consisting of a platform mounted on a wheeled frame, designed to transport patients and to allow for patient care before, during and after transport.

This recall has been terminated (originally issued September 16, 2008).

Company
Hill-Rom, Inc.
Recall Initiated
April 3, 2008
Posted
September 16, 2008
Terminated
December 29, 2009
Recall Number
Z-1655-2008
Quantity
564
Firm Location
Batesville, IN
Official Source
View on FDA website ↗

Reason for Recall

The auto contour function on/off handle may be inadvertently activated while the head of the stretcher is raised, increasing the possibility of the head section to become jammed and preventing it from lowering. This may result in a delay to the procedure.

Distribution

Worldwide Distribution --- including USA and countries of Australia, Belgium, Canada, France, Germany, Israel, Italy, Netherlands, Spain, Switzerland and United Kingdom.

Lot / Code Info

All units with serial numbers H352AN3566 through I222AN9588 and shipped prior to 8/13/07.

Root Cause

Device Design

Action Taken

Consignees will be visited to correct the problem and notified via a hand delivered Device Modification letter dated 4/3/08 at the time of the visit. If you have any questions please contact Jeffrey C. Shaul, Director, RA/QA Acute Care at (812) 931-2604.

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