Medartis APTUS — Class II medical device recall Z-2361-2026
Ongoing recall by Medartis AG, reported 2026-06-17, distributed nationwide. The cannulation of the CCS screw is not centered.
| Recall number | Z-2361-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medartis AG, Basel Town, N/A, Switzerland |
| Recall initiated | 2026-04-24 |
| Classified | 2026-06-09 |
| Reported by FDA | 2026-06-17 |
| Distributed | Nationwide (US) |
| Quantity | 13 units |
| UPC / GTIN / UDI-DI | 07630037887706 |
| Lot numbers | 24404471, 24425542, 25441997, 25444702 |
| Model numbers | 1/PKG, A-8216.50/1 |
Product
Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm, REF A-8216.50/1, 1/Pkg; Cannulated Compression Screws for bone fixation
Reason for recall
The cannulation of the CCS screw is not centered.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2361-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.