Hill-Rom, Inc. 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. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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.
Brand
Hill-Rom, Inc.
Lot Codes / Batch Numbers
All units with serial numbers H352AN3566 through I222AN9588 and shipped prior to 8/13/07.
Products Sold
All units with serial numbers H352AN3566 through I222AN9588 and shipped prior to 8/13/07.
Hill-Rom, Inc. is recalling Hill-Rom Procedural Stretcher with auto-contour option; Model P8000F. Wheeled hospital stretcher co due to The auto contour function on/off handle may be inadvertently activated while the head of the stretcher is raised, increasing the possibility of the he. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026