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Terminated

RotoProne powered patient rotation bed, part #209500, distributed by Kinetic Concepts, Inc., San Antonio, TX.

FDA Recall Z-0520-06 · Posted 2006-02-14

Recalling FirmKinetic Concepts, Inc
Recall StatusTerminated
Product CodeIKZ
Date Initiated2005-01-24
Date Terminated2006-06-29
Product Quantity91

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.

Firm Action

All KCI Service Centers notified via Technical Bulletin of upgrades. 1/24/2005

Root Cause

Other

Distribution Pattern

Devices distributed nationwide.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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