Prodisc C SK U: recall status

⚠ Recalls found. Prodisc C SK U is named in 2 official recalls in our current data:

FDA Class II recall Z-2050-2026 — Product labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm product was labeled as a 6mm.
FDA Class II recall Z-2051-2026 — Product labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm product was labeled as a 6mm.

Brand: Centinel Spine

Recalls naming this model

FDA Class II · Medical device · May 13, 2026

Prodisc C SK U recall — Centinel Spine, Inc.

Product labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm product was labeled as a 6mm.

Company / brand: Centinel Spine recalls

Affected product: Prodisc C SK U recall status

Official ID Z-2050-2026 · Official record ↗

FDA Class II · Medical device · May 13, 2026

Prodisc C SK U recall — Centinel Spine, Inc.

Product labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm product was labeled as a 6mm.

Company / brand: Centinel Spine recalls

Affected product: Prodisc C SK U recall status

Official ID Z-2051-2026 · Official record ↗

See all Centinel Spine 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.