Z-0402-05

Hill-Rom brand VersaCare Bed; product P3200

Name: Z-0402-05 Hill-Rom brand VersaCare Bed; product P3200
Creator: Hill-Rom, Inc.
Published: 2004-12-29
License: https://open.fda.gov/license/

Hill-Rom Inc. / initiated 2004-12-29 / Terminated

FDA source

Hill-Rom, Inc. began a recall of Hill-Rom brand VersaCare Bed; product P3200 on 2004-12-29. The reason FDA records is "A potential trip hazard exists when the fracture frame adaptor bracket is installed on the bed without the fracture frame". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0402-05
Status: Terminated
Initiated: 2004-12-29
Posted: 2005-01-15
Terminated: 2005-05-09
Recalling firm: Hill-Rom Inc.
Product: Hill-Rom brand VersaCare Bed; product P3200.
Product code: FNL Bed, Ac-Powered Adjustable Hospital
Reason for recall: A potential trip hazard exists when the fracture frame adaptor bracket is installed on the bed without the fracture frame.
FDA root cause: Other
Action: Customers were notified via letter dated 12/29/04 and informed of the hazard. Hill-Rom will visit each account to place instruction labels on the beds.
Quantity in commerce: 324
Distribution: Nationwide.
Product codes and lots: All serial numbers distributed prior to November 22, 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)