Recall Z-2453-2016— Biomet 3i, LLC

Class II · Terminated

Class II FDA medical device recall by Biomet 3i, LLC, initiated 2015-11-25, terminated 2019-07-26. FDA's recall record names no specific 510(k) clearance for this event. Product: Conical EP Pick-Up Coping (Hexed) Dental implants. Reason: Pouches may not have been sealed during packing..

Recalling firm
Biomet 3i, LLC
Classification
Class II
Status
Terminated
Initiated
2015-11-25
Terminated
2019-07-26
Firm location
Palm Beach Gardens, FL, United States

Product description

Conical EP Pick-Up Coping (Hexed) Dental implants

Reason for recall

Pouches may not have been sealed during packing.

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