SeaSpine Mariner Deformity Product Name: recall status

Notice names this product. SEASPINE ORTHOPEDICS’s SeaSpine Mariner Deformity Product Name is named in FDA Class II recall Z-3226-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: The proximal thread depth of the spinal device is out of design specification. Identifying details: UDI-DI 10889981257248; Affected Lots: TE145060D, TE170356F, TE170556F, TE165793F, TE145059E, TE161254F, TE142282D.. Units affected: 270 units. Status: Ongoing.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named: SeaSpine Mariner Deformity Product Name
Company / brand: SEASPINE ORTHOPEDICS
Lot / serial / date codes: UDI-DI 10889981257248; Affected Lots: TE145060D, TE170356F, TE170556F, TE165793F, TE145059E, TE161254F, TE142282D.
Distribution: US Nationwide distribution in the states of Alabama, California, Colorado, Connecticut, Florida, Georgia, Massachusetts, Michigan, Minnesota, Missouri, North Carolina, Nevada, New York, Oklahoma, Oregon, Tennessee, Texas, and Virginia.

Agency product description and boundaries

SeaSpine Mariner Deformity Product Name: Extended Polyaxial Head, Attached Gimbal, 12mm REF: MD1-300010-12

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

Brand: SEASPINE ORTHOPEDICS

Recalls naming this model

FDA Class II · Medical device · September 30, 2026

SeaSpine Mariner Deformity Product Name recall — SEASPINE ORTHOPEDICS CORPORATION

The proximal thread depth of the spinal device is out of design specification.

Company / brand: SEASPINE ORTHOPEDICS recalls

Affected product: SeaSpine Mariner Deformity Product Name recall status

Official ID Z-3226-2026 · Official record ↗

See all SEASPINE ORTHOPEDICS recalls →

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 6:00 PM UTC.