LEGION — Class II medical device recall Z-2624-2017
Terminated recall by Smith & Nephew, Inc., reported 2017-07-05, distributed in TN. The incorrect Loctite adhesive was used to assemble the impactor heads.
| Recall number | Z-2624-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Smith & Nephew, Inc., Memphis, TN, United States |
| Recall initiated | 2017-05-30 |
| Classified | 2017-06-23 |
| Reported by FDA | 2017-07-05 |
| Terminated | 2021-12-10 |
| Distributed | TN |
| Quantity | 36 units |
| Model numbers | 18MM, 20MM, 22MM, 71441976, 71441977, 71441978 |
Product
LEGION(R) FEM CONE IMPACTOR HEADS: a) REF 71441976, ID 18MM b) REF 71441977, ID 20MM c) REF 71441978, ID 22MM
Reason for recall
The incorrect Loctite adhesive was used to assemble the impactor heads.
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-2624-2017. 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.