FDA Device recall Z-0200-2019
Smith+Nephew Orthopaedic Division LEGION A/P FEMORAL CUTTING BLOCK, SIZE 6 REF 71434411, QTY: (1) The LEGION AP Femoral Cutting Block is a…
- FDA Device
- Class II
- terminated
- Published 2018-10-31
On 2018-10-31 the FDA classified a Class II recall of Smith+Nephew Orthopaedic Division LEGION A/P FEMORAL CUTTING BLOCK, SIZE 6 REF 71434411, QTY: (1) The LEGION AP Femoral Cutting Block is a… by Smith And Nephew, citing one lot of the Legion AP femoral cutting block, size 6, was manufactured with an oversized spring.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0200-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-09-18 |
| Published | 2018-10-31 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Smith And Nephew |
| Distribution | KS, TN |
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
One lot of the Legion AP femoral cutting block, size 6, was manufactured with an oversized spring.
Identifiers
| code_info | Lot 17LM05396 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0200-2019%22
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