Z-0661-05

Hill-Rom TotalCare SpO2RT pulmonary therapy bed system, Model 1900

Name: Z-0661-05 Hill-Rom TotalCare SpO2RT pulmonary therapy bed system, Model 1900
Creator: Hill-Rom, Inc.
Published: 2005-03-01
License: https://open.fda.gov/license/

Hill-Rom Inc. / initiated 2005-03-01 / Terminated

FDA source

Hill-Rom, Inc. began a recall of Hill-Rom TotalCare SpO2RT pulmonary therapy bed system, Model 1900 on 2005-03-01. The reason FDA records is "Siderails may stay up without latching into place". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0661-05
Status: Terminated
Initiated: 2005-03-01
Posted: 2005-03-30
Terminated: 2005-07-18
Recalling firm: Hill-Rom Inc.
Product: Hill-Rom TotalCare SpO2RT pulmonary therapy bed system, Model 1900.
Product code: FNL Bed, Ac-Powered Adjustable Hospital
Reason for recall: Siderails may stay up without latching into place.
FDA root cause: Other
Action: Consignees were notified via letter dated March 1, 2005 that Hill-Rom will contact them to coordinate a visit by Hill-Rom to upgrade affected beds.
Quantity in commerce: 228 beds
Distribution: Nationwide and Canada.
Product codes and lots: All beds modified [to convert other beds to the TotalCare SpO2RT pulmonary therapy bed systems] with upgrade kits P1950A01 or P1950A02 between February 2002 and November 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)