FDA Medical Device Recalls (openFDA)
Hill-Rom, Inc.: Hill-Rom brand TotalCare bed system; model P1900 -remanufactured only.
- Recall number
- Z-0761-04
- Recalling firm
- Hill-Rom, Inc.
- Product
- Hill-Rom brand TotalCare bed system; model P1900 -remanufactured only.
- Status
- Terminated
- Initiated
- 2004-03-15
- Posted
- 2004-07-20
- Terminated
- 2004-05-14
- Reason
- A warning label, advising users not to use oxygen tents with this equipment because of the potential for a fire, was not placed on these remanufactured beds.
- Root cause
- Other
- Action
- A letter dated 3/15/04 was sent to each affected consignee, with labels included, requesting that they attach them to each affected bed.
- Quantity
- 52
- Distribution
- Arizona, Florida, Georgia, Nevada, Puerto Rico, Texas, Virginia and Canada.
- Lot, serial or model codes
- All remanufactured beds distributed between August 2003 and February 2004.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- LLI
- Firm FEI
- 1824206
- Firm city
- Batesville
- Firm state
- IN
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28