Z-0206-04

Hill-Rom brand Resident LT bed ambulatory assist bar accessory; accessory P865A

Name: Z-0206-04 Hill-Rom brand Resident LT bed ambulatory assist bar accessory; accessory P865A
Creator: Hill-Rom, Inc.
Published: 2003-11-14
License: https://open.fda.gov/license/

Hill-Rom Inc. / initiated 2003-11-14 / Terminated

FDA source

Hill-Rom, Inc. began a recall of Hill-Rom brand Resident LT bed ambulatory assist bar accessory; accessory P865A on 2003-11-14. The reason FDA records is "The ambulatory assist bar may not lock into position and may come out of place due to incorrect assembly". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0206-04
Status: Terminated
Initiated: 2003-11-14
Posted: 2003-12-10
Terminated: 2004-08-06
Recalling firm: Hill-Rom Inc.
Product: Hill-Rom brand Resident LT bed ambulatory assist bar accessory; accessory P865A.
Product code: KMM
Reason for recall: The ambulatory assist bar may not lock into position and may come out of place due to incorrect assembly.
FDA root cause: Other
Action: Customers were advised of the recall by letter dated 11/12/03 and mailed on 11/14/03. A Hill-Rom representative will visit each customer to assure the latching mechanism is properly attached to the bed.
Quantity in commerce: 1400
Distribution: United States and Canada
Product codes and lots: All units distributed between March 1997 and September 2003.

Product code KMM

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)