APTUS 2 — Class II medical device recall Z-1821-2024
Ongoing recall by Medartis Inc., reported 2024-05-22, distributed nationwide. Screw is 16mm long instead of 22mm long.
| Recall number | Z-1821-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medartis Inc., Warsaw, IN, United States |
| Recall initiated | 2024-04-12 |
| Classified | 2024-05-14 |
| Reported by FDA | 2024-05-22 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CH, CZ, DE, FI, FR, PL, ZA |
| Quantity | 110 units |
| Lot numbers | 24377397 |
| Model numbers | A-5850.22/1 |
Product
APTUS 2.8 TriLock Screw 22mm, HD7, 1/Pkg. Metal bone fixation fastener used with the APTUS fixation system.
Reason for recall
Screw is 16mm long instead of 22mm long.
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-1821-2024. 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.