FDA Class II · Medical device · June 17, 2026
Medartis APTUS recall — Medartis AG
The cannulation of the CCS screw is not centered.
Official ID Z-2361-2026 · Official record ↗
Medartis AG recalls
Recall found. Medartis AG is named in FDA Class II recall Z-2361-2026 covering Medartis APTUS. Hazard: The cannulation of the CCS screw is not centered. Identifying details: UDI/DI 07630037887706, Lot Numbers: 25444702, 24425542, 24404471, 25441997. Status: Ongoing.
Models with recalls
All Medartis AG recalls
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- Recalls.gov — the U.S. government’s all-agency portal ↗
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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.