Z-0810-04

Magnum II Bariatric Patient Care System

Name: Z-0810-04 Magnum II Bariatric Patient Care System
Creator: Hill-Rom Manufacturing, Inc.
Published: 2004-03-04
License: https://open.fda.gov/license/

Hill-Rom Manufacturing, Inc. / initiated 2004-03-04 / Terminated

FDA source

Hill-Rom Manufacturing, Inc. began a recall of Magnum II Bariatric Patient Care System on 2004-03-04. The reason FDA records is "Bed may pose a health hazard due to: A) Inability to articulate the frame during transport, B) Exposed sharp edge of footplate, C) Shear point between seat section and lymph panel and D) Patient fall". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0810-04
Status: Terminated
Initiated: 2004-03-04
Posted: 2004-07-20
Terminated: 2005-05-24
Recalling firm: Hill-Rom Manufacturing, Inc.
Product: Magnum II Bariatric Patient Care System
Product code: FNL Bed, Ac-Powered Adjustable Hospital
Reason for recall: Bed may pose a health hazard due to: A) Inability to articulate the frame during transport, B) Exposed sharp edge of footplate, C) Shear point between seat section and lymph panel and D) Patient fall.
FDA root cause: Other
Action: Consignees were notified by letter via Federal Express on 3/9/2004.
Quantity in commerce: 1424 units
Distribution: The Magnum II Bariatric Patient System is primarily leased by hospitals, although some units have been sold Nationwide and Canada.
Product codes and lots: Serial No. FTxxxxxx (where xxxxxx is a 6-digit number sequence)

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)