Drug recall
Centered Glenosphere w/Screw, CoCr/TA6V/TiN 10-degrees Tilt 32 mm, REF: 115-3210
FDA recall event 93729 · Class II · FX SHOULDER
Key facts
| Event ID | 93729 |
|---|---|
| Recall numbers | Z-0843-2024 |
| Recalling firm | FX SHOULDER |
| Product type | Devices |
| Products | Centered Glenosphere w/Screw, CoCr/TA6V/TiN 10-degrees Tilt 32 mm, REF: 115-3210 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Centered glenosphere box may contain an eccentric glenosphere. |
| Initiation date | Aug 8, 2023 |
| Report date | Feb 7, 2024 |
| City | Dallas |
| State | TX |
| Country | United States |
| FEI number | 3014128390 |
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: