FDAOctober 30, 2015device

RBT, Internal Implant, Laser-Lok, 5.0 x 15mm, 5.7 Platform, REF LPBR5015, Rx only, Sterile R, BIOHORIZONS(R), Dental Implant

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

The hazard

An incorrect label reading 10.5mm and not the specified 15mm was placed on the implant inner vial packaging.

What to do

FDA enforcement status: Terminated

Brands named

biohorizons implant systemsbiohorizonsbiohorizons implant

Recall history

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

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