FDAAugust 6, 2025device

Reef TA Inserter, Part Number: TA2-001003, part of the Reef Interbody System

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

The hazard

Inserter, used as part of a system with an intervertebral body fusion device, may contribute to difficulty disengaging the implant or improper implant positioning, which may may lead to prolonged surgery, intraoperative revision, and may require the use of alternate instrumentation. Devices may also have incorrect UDI-DI marking.

What to do

FDA enforcement status: Ongoing

Brands named

seaspine orthopedicsseaspine

UPCs

1088998129073310889981437800

Recall history

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

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Reef TA Inserter, Part Number: TA2-001003, part of the Reef Interbody System — Recall Details · AllClear