Skytron General Purpose Surgical Table, battery model; Model 6600B, Dist. by Skytron, Grand Rapids, MI.
FDA device recall Z-1497-06 · 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
Monitor recalls programmatically
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| SKYTRON SKYBOOM SERIES (K950192) | Skytron, Div. the Kmw Group, Inc. | 1995-04-03 |