Drug recall
Syntel Silicone Thrombectomy Catheter, Sterile, Rx Only. Used in vascular grafts and peripheral venous…
FDA recall event 94457 · Class II · LeMaitre Vascular, Inc.
Key facts
| Event ID | 94457 |
|---|---|
| Recall numbers | Z-1824-2024 |
| Recalling firm | LeMaitre Vascular, Inc. |
| Product type | Devices |
| Products | Syntel Silicone Thrombectomy Catheter, Sterile, Rx Only. Used in vascular grafts and peripheral venous thrombectomies. |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The guide tip can become damaged and result in the tip detaching. |
| Initiation date | Apr 17, 2024 |
| Report date | May 22, 2024 |
| City | Burlington |
| State | MA |
| Country | United States |
| FEI number | 1220948 |
At a glance
- 1–9 Products in this recall
- 10–99 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: