Smith+Nephew Orthopaedic Division LEGION A/P FEMORAL CUTTING BLOCK — Class II medical device recall Z-0200-2019
Terminated recall by Smith & Nephew, Inc., reported 2018-10-31, distributed in KS, TN. One lot of the Legion AP femoral cutting block, size 6, was manufactured with an oversized spring.
| Recall number | Z-0200-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Smith & Nephew, Inc., Memphis, TN, United States |
| Recall initiated | 2018-09-18 |
| Classified | 2018-10-22 |
| Reported by FDA | 2018-10-31 |
| Terminated | 2019-05-08 |
| Distributed | KS, TN |
| Quantity | 6 units |
| Lot numbers | 17LM05396 |
| Model numbers | 71434411 |
Product
Smith+Nephew Orthopaedic Division LEGION A/P FEMORAL CUTTING BLOCK, SIZE 6 REF 71434411, QTY: (1) The LEGION AP Femoral Cutting Block is a reusable surgical instrument used to make bone cuts on the distal femur to prepare the bone to receive a LEGION femoral implant.
Reason for recall
One lot of the Legion AP femoral cutting block, size 6, was manufactured with an oversized spring.
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-0200-2019. 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.