FDA Medical Device Recalls (openFDA)
Kinetic Concepts, Inc: RotoProne powered patient rotation bed, part #209500, distributed by Kinetic Concepts, Inc., San Antonio, TX.
- Recall number
- Z-0520-06
- Recalling firm
- Kinetic Concepts, Inc
- Product
- RotoProne powered patient rotation bed, part #209500, distributed by Kinetic Concepts, Inc., San Antonio, TX.
- Status
- Terminated
- Initiated
- 2005-01-24
- Posted
- 2006-02-14
- Terminated
- 2006-06-29
- Reason
- To correct software issues in software versions 1.3 and 1.5 and to upgrade hatch latch handles to a more ergonomic design.
- Root cause
- Other
- Action
- All KCI Service Centers notified via Technical Bulletin of upgrades. 1/24/2005
- Quantity
- 91
- Distribution
- Devices distributed nationwide.
- Lot, serial or model codes
- Serial Numbers: RRFK00036 - RRFK00128.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- IKZ
- Firm FEI
- 1625774
- Firm city
- San Antonio
- Firm state
- TX
- 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