Drug recall
stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty
FDA recall event 94194 · Class II · Wright Medical Technology, Inc.
Key facts
| Event ID | 94194 |
|---|---|
| Recall numbers | Z-1477-2024 |
| Recalling firm | Wright Medical Technology, Inc. |
| Product type | Devices |
| Products | stryker Infinity Resection Adjustment Block, REF 33600030, ankle arthroplasty |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Stryker has identified an issue that impacts specific lots of Infinity" Resection Guide Adjustment Blocks. The parts within these three lots were found to have been missing an internal screw in the… |
| Initiation date | Mar 6, 2024 |
| Report date | Apr 10, 2024 |
| 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: