Thermoplastic templates, free-end situation Catalog Number: 040.527
FDA device recall Z-0603-06 · posted 2006-03-09 · Terminated
Recall details
- Recalling firm
- Straumann Manufacturing Inc.
- Reason for recall
- Pilot drills may not fully extend through drill guide in template products
- Action taken
- Straumann USA notified consignees by letter dated 1/30/06 requesting return of the devices.
- Root cause
- Other
- Status
- Terminated
- Product code
- DZJ
- Quantity affected
- 22
- Distribution
- Nationwide
- Date initiated
- 2006-01-30
- Date posted
- 2006-03-09
- Date terminated
- 2006-05-04
- Location
- Andover, MA
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