Class II — Medartis AG
| Recalling firm | MEDARTIS AG |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | The cannulation of the CCS screw is not centered. |
| Product | Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm, REF A-8216.50/1, 1/Pkg; Cannulated Compression Screws for bone fixation |
| Quantity | 13 units |
| Distribution | US Nationwide distribution in the states of LA, TX. IN, CA, NC. |
| Initiated | 2026-04-24 |
| Classified | 2026-06-09 |
| Recall number | Z-2361-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Medartis AG (Z-2361-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/98952/
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