FDAMay 18, 2018device

REPLANT 5.0mmD ABUTMENT, Part number 6050-52-60

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Due to out of specification, the clinician would not be able to fit and engage the abutment with the implant

What to do

FDA enforcement status: Terminated

Brands named

implant direct sybron manufacturingimplantimplant direct

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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