FDANovember 22, 2019device
LOCATOR OVERDENTURE IMPLANT SYSTEM STERILE R Rx Only QTY 1 .
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The abutment provided with the Implant System may be out of specification, which could lead to a small gap occurring between the implant and abutment on assembly in the patient.
What to do
FDA enforcement status: Ongoing
Brands named
zest anchorszest
UPCs
0084048110149600840481101526008404811015710084048110159500840481126116
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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