Drug recall
LEGION NARROW PS OXIN SZ 6N RT and JRNY II BCS FEMORAL OXIN LT SZ 5
FDA recall event 90078 · Class II · Smith & Nephew Inc
Key facts
| Event ID | 90078 |
|---|---|
| Recall numbers | Z-1099-2022 |
| Recalling firm | Smith & Nephew Inc |
| Product type | Devices |
| Products | LEGION NARROW PS OXIN SZ 6N RT and JRNY II BCS FEMORAL OXIN LT SZ 5 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| 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. |
| Initiation date | Apr 19, 2022 |
| Report date | May 25, 2022 |
| Termination date | Aug 16, 2024 |
| City | Memphis |
| State | TN |
| Country | United States |
| FEI number | 3005551626 |
At a glance
- 1–9 Products in this recall
- 1–9 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: