Fresh Recalls

SEASPINE ORTHOPEDICS recalls

Recall found. SEASPINE ORTHOPEDICS is named in FDA Class II recall Z-2762-2026 covering SeaSpine Polyaxial Head REF Number. Hazard: Due to manufacturing error, polyaxial head may popoff from the screw intraoperatively following insertion. Identifying details: UDI: 10889981155117; Affected Lots: AW199682G, AW199684G.. Status: Ongoing.

Models with recalls

SeaSpine Polyaxial Head REF Number (1)

All SEASPINE ORTHOPEDICS recalls

FDA Class II · Medical device · July 29, 2026

SeaSpine Polyaxial Head REF Number recall — SEASPINE ORTHOPEDICS CORPORATION

Due to manufacturing error, polyaxial head may popoff from the screw intraoperatively following insertion.

Official ID Z-2762-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked September 7, 2026 at 6:00 AM UTC.