FDA Medical Device Recalls (openFDA)
Hill-Rom, Inc.: Hill-Rom Newborn bassinet; model P248.
- Recall number
- Z-0303-04
- Recalling firm
- Hill-Rom, Inc.
- Product
- Hill-Rom Newborn bassinet; model P248.
- Status
- Terminated
- Initiated
- 2003-12-19
- Posted
- 2004-01-08
- Terminated
- 2004-09-14
- Reason
- The caster/wheel may come off of the bassinet, causing the bassinet to tip.
- Root cause
- Other
- Action
- Recall letters dated December 19, 2003 were sent to each customer. Customers were instructed to verify the security of the casters to the base, and to visually check for loose or missing caster screws until Hill-Rom can visit each facility and perform a fix.
- Quantity
- not on file
- Distribution
- United States, Australia, Canada, China, France, Germany, Honduras, Israel, Japan, Mexico, Panama, Taiwan, Turkey, United Arab Emirates and United Kingdom.
- Lot, serial or model codes
- All units distributed between May 1989 and March 2001.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FMS
- 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