Recall Z-0267-2016— Biomet 3i, LLC

Class II · Terminated

Class II FDA medical device recall by Biomet 3i, LLC, initiated 2015-08-10, terminated 2016-10-12. FDA's recall record names no specific 510(k) clearance for this event. Product: Biomet 3i Narrow Right Angle Square Driver Tip. Driver tips are attached to a surgical drilling unit to carry components such as implant mounts, healing abutments and screws for placement and removal. For dental and restorative procedures.. Reason: RASQ3N, a square, abutment screw driver tip has been labeled and distributed as RASH3N, a hexed, abutment screw driver tip. Additionally, the RASQ3N received the RASH3N's laser marking "RASH3N" during manufacturing..

Recalling firm
Biomet 3i, LLC
Classification
Class II
Status
Terminated
Initiated
2015-08-10
Terminated
2016-10-12
Firm location
Palm Beach Gardens, FL, United States

Product description

Biomet 3i Narrow Right Angle Square Driver Tip. Driver tips are attached to a surgical drilling unit to carry components such as implant mounts, healing abutments and screws for placement and removal. For dental and restorative procedures.

Reason for recall

RASQ3N, a square, abutment screw driver tip has been labeled and distributed as RASH3N, a hexed, abutment screw driver tip. Additionally, the RASQ3N received the RASH3N's laser marking "RASH3N" during manufacturing.

Data sourced from openFDA. This site is unofficial and independent of the FDA.