FDA Medical Device Recalls (openFDA)
Hill-Rom Manufacturing, Inc.: Clinitron At Home Air Fluidized Therapy Bed
- Recall number
- Z-1555-05
- Recalling firm
- Hill-Rom Manufacturing, Inc.
- Product
- Clinitron At Home Air Fluidized Therapy Bed
- Status
- Terminated
- Initiated
- 2005-05-20
- Posted
- 2005-09-21
- Terminated
- 2006-04-26
- Reason
- Sudden unexpected lowering of the head of the bed may occur due to failure of the had of the bed actuator.
- Root cause
- Other
- Action
- Customer letter was hand delivered to consignees by Hill-Rom Service Technicians 05/20/2005. The affected product will be corrected by replacement of the actuator with one from an unaffected lot.
- Quantity
- 21 beds
- Distribution
- AL, FL, KY, LA, MA, NC, NY, TN, TX, VA
- Lot, serial or model codes
- Serial numbers: CS102304, CS103257, CS103901, CS103902, CS103903, CS103904, CS103909, CS103911, CS103914, CS103915, CS103916, CS103917, CS103919, CS103921, CS103923, CS103924, CS103925, CS103928, CS103932, CS103933.
- 510(k) numbers
- ["K942184"]
- PMA numbers
- not on file
- Product code
- FNL
- 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