FDAFebruary 23, 2018device

ORTHOFIX, Connector System, LARGE SET SCREW, REF 79-2002

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

The hazard

Orthofix is conducting a voluntary recall of the Connector System Large Set Screw (PN: 79-2002) with affected Lot Numbers 001 and 002, and Small Set Screw (PN: 79-2003) with affected Lot Numbers 002, 003 and 004. Through the company's manufacturing controls, size discrepancies were noted with the drive feature for both the large and small sets screws. As a result, it is possible that (1) the set screw drive feature will not accept the Set Screw Driver (PN: 79-1006) or (2) the driver may get wedged in the corners of the drive feature (false bottom) which may lead to a stripped set screw.

What to do

FDA enforcement status: Terminated

Brands named

orthofix

UPCs

18257200125364

Recall history

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

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ORTHOFIX, Connector System, LARGE SET SCREW, REF 79-2002 — Recall Details · AllClear