Z-0338-04

Hill-Rom brand Century+ bed; model P1400

Name: Z-0338-04 Hill-Rom brand Century+ bed; model P1400
Creator: Hill-Rom, Inc.
Published: 2003-12-26
License: https://open.fda.gov/license/

Hill-Rom Inc. / initiated 2003-12-26 / Terminated

FDA source

Hill-Rom, Inc. began a recall of Hill-Rom brand Century+ bed; model P1400 on 2003-12-26. The reason FDA records is "If fluid is spilled on the siderail or the bed control areas, the bed may change positions without user input". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0338-04
Status: Terminated
Initiated: 2003-12-26
Posted: 2004-01-10
Terminated: 2004-05-13
Recalling firm: Hill-Rom Inc.
Product: Hill-Rom brand Century+ bed; model P1400.
Product code: FNL Bed, Ac-Powered Adjustable Hospital
Reason for recall: If fluid is spilled on the siderail or the bed control areas, the bed may change positions without user input.
FDA root cause: Other
Action: A recall letter dated December 26, 2003 was sent to each customer. Customers are asked to follow instructions in the user manual, if there is a fluid spill onto a unit, until Hill-Rom can inspect each unit to determine whether it is affected by the problem.
Quantity in commerce: 222
Distribution: United States, Canada , Panama and Taiwan.
Product codes and lots: All beds distributed between August 3, 2003 and August 20, 2003.

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)