Atlas FDA

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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