FDA Medical Device Recalls (openFDA)
Hill-Rom, Inc.: Hill-Rom 100 Low Bed; Model No. P3930.
- Recall number
- Z-1603-2008
- Recalling firm
- Hill-Rom, Inc.
- Product
- Hill-Rom 100 Low Bed; Model No. P3930.
- Status
- Terminated
- Initiated
- 2008-04-08
- Posted
- 2008-09-05
- Terminated
- 2010-10-13
- Reason
- The upper deck may collapse to its lowest position and the caster brakes may fracture if the bed is moved while the brakes are locked.
- Root cause
- Device Design
- Action
- Consignees were notified via letter dated April 8, 2008 to lower these beds to their lowest position, to remove the beds from use if they move more than 1/2 inch with the brakes locked and that the firm will repair these beds when fixes become available. If you have questions regarding this recall, contact Hill-Rom Technical Support at 800-445-3730.
- Quantity
- 753 beds
- Distribution
- Worldwide: USA and Canada.
- Lot, serial or model codes
- All units.
- 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