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
All SEASPINE ORTHOPEDICS recalls
FDA Class II · Medical device · July 29, 2026
Due to manufacturing error, polyaxial head may popoff from the screw intraoperatively following insertion.
Official ID Z-2762-2026 ·
Official record ↗
Compiled from official public-domain government data. Last checked September 7, 2026 at 6:00 AM UTC.