FDA Medical Device Recalls (openFDA)
Kreuzer Gmbh & Co. KG: klinoPORT, AC powered Operating Table
- Recall number
- Z-0802-2011
- Recalling firm
- Kreuzer Gmbh & Co. KG
- Product
- klinoPORT, AC powered Operating Table
- Status
- Terminated
- Initiated
- 2010-10-26
- Posted
- 2010-12-22
- Terminated
- 2012-03-20
- Reason
- The motorized adjustable pendant arm may suddenly descend to its lowest position.
- Root cause
- Other
- Action
- Consignees were notified by a Warning Notice on/about 10/26/2010. Medical facilities were instructed to adjust the pendant arm to the lowest height position and disable the motor and to place the accompanying warning label on the pendant. They will, therefore, not be able to adjust the height of the pendant until corrective action is developed and completed. TRUMPF Medical Systems, Inc. will receive corrective action repair kits by 11/12/2010.
- Quantity
- 15 units
- Distribution
- Nationwide Distribution -- CT, MA, and MO.
- Lot, serial or model codes
- Model number: klinoPORT 706, 806, 906, 1006 and 1306, Serial number between: 101039290 and 101158669
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FQO
- Firm FEI
- 1000182014
- Firm city
- Puchheim
- Firm state
- not on file
- Firm country
- Germany
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
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
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