Drug recall
Smith+Nephew Orthopaedic Division LEGION A/P FEMORAL CUTTING BLOCK, SIZE 6 REF 71434411, QTY: (1) The LEGION…
FDA recall event 81100 · Class II · Smith & Nephew, Inc.
Key facts
| Event ID | 81100 |
|---|---|
| Recall numbers | Z-0200-2019 |
| Recalling firm | Smith & Nephew, Inc. |
| Product type | Devices |
| Products | 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… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | One lot of the Legion AP femoral cutting block, size 6, was manufactured with an oversized spring. |
| Initiation date | Sep 18, 2018 |
| Report date | Oct 31, 2018 |
| Termination date | May 8, 2019 |
| City | Memphis |
| State | TN |
| Country | United States |
| FEI number | 1020279 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: