Z-1603-2008

Hill-Rom 100 Low Bed; Model No. P3930

Name: Z-1603-2008 Hill-Rom 100 Low Bed; Model No. P3930
Creator: Hill-Rom, Inc.
Published: 2008-04-08
License: https://open.fda.gov/license/

Hill-Rom Inc. / initiated 2008-04-08 / Terminated / root cause: design

FDA source

Hill-Rom, Inc. began a recall of Hill-Rom 100 Low Bed; Model No. P3930 on 2008-04-08. The reason FDA records is "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". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as design.

Recall record

Recall number: Z-1603-2008
Status: Terminated
Initiated: 2008-04-08
Posted: 2008-09-05
Terminated: 2010-10-13
Recalling firm: Hill-Rom Inc.
Product: Hill-Rom 100 Low Bed; Model No. P3930.
Product code: FNL Bed, Ac-Powered Adjustable Hospital
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.
Root cause tag: design
FDA root cause: Device Design
Action: 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.
Quantity in commerce: 753 beds
Distribution: Worldwide: USA and Canada.
Product codes and lots: All units.

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)