Drug recall
Stryker INFINITY Resect Guide for INBONE Talus, Size 4, Model #33620254, non-sterile, an instrument used with…
FDA recall event 90216 · Class II · Wright Medical Technology, Inc.
Key facts
| Event ID | 90216 |
|---|---|
| Recall numbers | Z-1291-2022 |
| Recalling firm | Wright Medical Technology, Inc. |
| Product type | Devices |
| Products | Stryker INFINITY Resect Guide for INBONE Talus, Size 4, Model #33620254, non-sterile, an instrument used with the INFINITY Total Ankle System. |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The instrument is incorrectly color coded. |
| Initiation date | Jun 2, 2022 |
| Report date | Jul 6, 2022 |
| City | Memphis |
| State | TN |
| Country | United States |
| FEI number | 3010667733 |
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: