FDA Medical Device Recalls (openFDA)
Hill-Rom, Inc.: Hill-Rom brand VersaCare Bed; product P3200.
- Recall number
- Z-0402-05
- Recalling firm
- Hill-Rom, Inc.
- Product
- Hill-Rom brand VersaCare Bed; product P3200.
- Status
- Terminated
- Initiated
- 2004-12-29
- Posted
- 2005-01-15
- Terminated
- 2005-05-09
- Reason
- A potential trip hazard exists when the fracture frame adaptor bracket is installed on the bed without the fracture frame.
- Root cause
- Other
- Action
- Customers were notified via letter dated 12/29/04 and informed of the hazard. Hill-Rom will visit each account to place instruction labels on the beds.
- Quantity
- 324
- Distribution
- Nationwide.
- Lot, serial or model codes
- All serial numbers distributed prior to November 22, 2004.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FNL
- 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