LEGION NARROW PS OXIN SZ 6N RT and JRNY II BCS FEMORAL OXIN LT SZ 5 — Class II medical device recall Z-1099-2022
Terminated recall by Smith & Nephew Inc, reported 2022-05-25, distributed nationwide. It was reported that a JOURNEY II BCS Femoral OXIN LT SZ5 was in a box labelled as a LEGION NARROW PS OXIN SZ
| Recall number | Z-1099-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Smith & Nephew Inc, Memphis, TN, United States |
| Recall initiated | 2022-04-19 |
| Classified | 2022-05-16 |
| Reported by FDA | 2022-05-25 |
| Terminated | 2024-08-16 |
| Distributed | Nationwide (US) |
| Countries outside the US | JP |
| Quantity | 16 units |
| UPC / GTIN / UDI-DI | 00885556170410 |
| Lot numbers | 21JM17389, 21JM18618 |
| Model numbers | 71421276, 74022125 |
Product
LEGION NARROW PS OXIN SZ 6N RT and JRNY II BCS FEMORAL OXIN LT SZ 5
Reason for recall
It was reported that a JOURNEY II BCS Femoral OXIN LT SZ5 was in a box labelled as a LEGION NARROW PS OXIN SZ 6N RT.
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-1099-2022. 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.