FDA Medical Device Recalls (openFDA)
Hill-Rom Manufacturing, Inc.: CLINITRON UP-LIFT Air Fluidized Therapy unit.
- Recall number
- Z-0990-03
- Recalling firm
- Hill-Rom Manufacturing, Inc.
- Product
- CLINITRON UP-LIFT Air Fluidized Therapy unit.
- Status
- Terminated
- Initiated
- 2003-05-05
- Posted
- 2003-07-10
- Terminated
- 2004-07-26
- Reason
- Malfunction of side-rail latching pin coupled with inadequate directions for use.
- Root cause
- Other
- Action
- Consignees were notified by letter sent via Airborne express, on May 5, 2003. Side-rail latching pins will be replaced with a more robust version. Label indicating directions for use will be modified to include detailed information on proper procedures for moving the units.
- Quantity
- 122 units (including both units)
- Distribution
- The units are primarily leased to hospitals. Units have been sold to hospitals located nationwide and to Canada, Austria, France, Germany Ireland Italy, Netherlands, Spain, Sweden, Switzerland and the United Kingdom.
- Lot, serial or model codes
- Model: Uplift, Serial #CH(all numeric codes).
- 510(k) numbers
- ["K920112"]
- PMA numbers
- not on file
- Product code
- INX
- Firm FEI
- 1045510
- Firm city
- Charleston
- Firm state
- SC
- 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