Z-0726-04

Hill Rom brand Advanta bed; model P1600

Name: Z-0726-04 Hill Rom brand Advanta bed; model P1600
Creator: Hill-Rom, Inc.
Published: 2004-03-08
License: https://open.fda.gov/license/

Hill-Rom Inc. / initiated 2004-03-08 / Terminated

FDA source

Hill-Rom, Inc. began a recall of Hill Rom brand Advanta bed; model P1600 on 2004-03-08. The reason FDA records is "A potential pinch/shear point exists between the restraint strap hook located underneath the knee section and the foot rail mounting of the bed". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0726-04
Status: Terminated
Initiated: 2004-03-08
Posted: 2004-07-20
Terminated: 2004-09-02
Recalling firm: Hill-Rom Inc.
Product: Hill Rom brand Advanta bed; model P1600.
Product code: FNL Bed, Ac-Powered Adjustable Hospital
Reason for recall: A potential pinch/shear point exists between the restraint strap hook located underneath the knee section and the foot rail mounting of the bed.
FDA root cause: Other
Action: A recall letter dated March 8, 2004 was sent to each consignee advising them of the problem, and that Hill-Rom will visit the facility to modify the beds.
Quantity in commerce: 294
Distribution: California, Delaware, Idaho, Indiana, Massachusetts, Michigan, Mississippi, New York, North Carolina, Ohio, South Dakota, Tennesee and Canada.
Product codes and lots: All units distributed between January 1, 2004 and February 11, 2004.

Product code FNL

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)