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Terminated

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

FDA Recall Z-1496-06 · 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.

K950192SKYTRON SKYBOOM SERIESSkytron, Div. the Kmw Group, Inc. · 1995-04-03

Official Source

View FDA Recall →

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

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