Skip to the content

FDA Medical Device Recalls (openFDA)

Skytron, Div. The KMW Group, Inc: Skytron General Purpose Surgical Table, battery model; Model 6600B, Dist. by Skytron, Grand Rapids, MI.

Recall number
Z-1497-06
Recalling firm
Skytron, Div. The KMW Group, Inc
Product
Skytron General Purpose Surgical Table, battery model; Model 6600B, Dist. by Skytron, Grand Rapids, MI.
Status
Terminated
Initiated
2005-08-04
Posted
2006-09-13
Terminated
2008-05-01
Reason
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.
Root cause
Other
Action
A service bulletin was issued to distributors on 8/12/05 instructing them to identify customers and to retrofit these tables.
Quantity
160 total
Distribution
Nationwide.
Lot, serial or model codes
All units. Serial numbers 6600B-2D-002 through 6600B-2L-060.
510(k) numbers
["K950192"]
PMA numbers
not on file
Product code
FQO
Firm FEI
1825014
Firm city
Grand Rapids
Firm state
MI
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

Search this register