Drug recall
Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312
FDA recall event 95152 · Class II · Medtronic Perfusion Systems
Key facts
| Event ID | 95152 |
|---|---|
| Recall numbers | Z-3128-2024 |
| Recalling firm | Medtronic Perfusion Systems |
| Product type | Devices |
| Products | Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | During manufacturing, DLP Single Stage Venous Cannulae - straight tip (Model 66118) was incorrectly placed into a product labeled as DLP Single Stage Venous Cannulae - right angle metal tip (Model… |
| Initiation date | Jul 9, 2024 |
| Report date | Sep 18, 2024 |
| City | Brooklyn Park |
| State | MN |
| Country | United States |
| FEI number | 1000116158 |
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: