Atlas FDA

Arthrotek brand Lactoscrew instruments 3.5 mm drill bit, stainless steel; ref. 905585.

FDA device recall Z-0329-06 · posted 2005-12-28 · Terminated

Recall details

Recalling firm
Biomet, Inc.
Reason for recall
The bit may bend or fracture during use.
Action taken
Consignees were notified to return the product via letter dated 11/10/05.
Root cause
Other
Status
Terminated
Product code
GFG
Quantity affected
46
Distribution
Nationwide, Australia, Belgium, Columbia, Finland, Israel, Poland and United Kingdom.
Date initiated
2005-11-10
Date posted
2005-12-28
Date terminated
2006-01-12
Location
Warsaw, IN

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