Z-0948-05

Hill-Rom Century+ Bed, Model P1400

Name: Z-0948-05 Hill-Rom Century+ Bed, Model P1400
Creator: Hill-Rom, Inc.
Published: 2005-05-20
License: https://open.fda.gov/license/

Hill-Rom Inc. / initiated 2005-05-20 / Terminated

FDA source

Hill-Rom, Inc. began a recall of Hill-Rom Century+ Bed, Model P1400 on 2005-05-20. The reason FDA records is "Sleep bed pivot bolts may break, allowing the head section to shift or to drop to one side". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0948-05
Status: Terminated
Initiated: 2005-05-20
Posted: 2005-06-30
Terminated: 2005-08-12
Recalling firm: Hill-Rom Inc.
Product: Hill-Rom Century+ Bed, Model P1400.
Product code: FNL Bed, Ac-Powered Adjustable Hospital
Reason for recall: Sleep bed pivot bolts may break, allowing the head section to shift or to drop to one side.
FDA root cause: Other
Action: Consignees were notified via letter dated 5/20/05 that the firm will visit consignees to make corrections to the beds.
Quantity in commerce: 218
Distribution: Nationwide (California, District of Columbia, Florida, Massachusetts, Montana, Nevada, New Jersey, New York, Pennsylvania, Texas, Virginia), Brazil and Canada.
Product codes and lots: Beds built between March 2005 and May 2005.

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)