RotoProne powered patient rotation bed, part #209500, distributed by Kinetic Concepts, Inc., San Antonio, TX.
FDA device recall Z-0520-06 · posted 2006-02-14 · Terminated
Recall details
- Recalling firm
- Kinetic Concepts, Inc
- Reason for recall
- To correct software issues in software versions 1.3 and 1.5 and to upgrade hatch latch handles to a more ergonomic design.
- Action taken
- All KCI Service Centers notified via Technical Bulletin of upgrades. 1/24/2005
- Root cause
- Other
- Status
- Terminated
- Product code
- IKZ
- Quantity affected
- 91
- Distribution
- Devices distributed nationwide.
- Date initiated
- 2005-01-24
- Date posted
- 2006-02-14
- Date terminated
- 2006-06-29
- Location
- San Antonio, TX
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