Skytron General Purpose Surgical Table, battery model; Model 6600B, Dist. by Skytron, Grand Rapids, MI.
FDA Recall Z-1497-06 · Posted 2006-09-13
Recalling FirmSkytron, Div. The KMW Group, Inc
Recall StatusTerminated
Product CodeFQO
Date Initiated2005-08-04
Date Terminated2008-05-01
Product Quantity160 total
Reason for Recall
The release levers can inadvertently release under load while the leg section is positioned at a ninety degree angle causing the leg section to drop.
Firm Action
A service bulletin was issued to distributors on 8/12/05 instructing them to identify customers and to retrofit these tables.
Root Cause
Other
Distribution Pattern
Nationwide.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.