Atlas FDA

Skytron General Purpose Surgical Table; Model 6600, Dist. by Skytron, Grand Rapids, MI.

FDA device recall Z-1496-06 · posted 2006-09-13 · Terminated

Recall details

Recalling firm
Skytron, Div. The KMW Group, Inc
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.
Action taken
A service bulletin was issued to distributors on 8/12/05 instructing them to identify customers and to retrofit these tables.
Root cause
Other
Status
Terminated
Product code
FQO
Quantity affected
160 total
Distribution
Nationwide.
Date initiated
2005-08-04
Date posted
2006-09-13
Date terminated
2008-05-01
Location
Grand Rapids, MI

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Related 510(k) clearances

RecordFirmDate
SKYTRON SKYBOOM SERIES (K950192)Skytron, Div. the Kmw Group, Inc.1995-04-03