Medtronic Perfusion Systems Recall: Medtronic Left Heart Vent Catheters: a) DLP¿ Intracard
Medtronic Perfusion Systems Recall: Medtronic Left Heart Vent Catheters: a) DLP¿ Intracard is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Medtronic Perfusion Systems; Product: Medtronic Left Heart Vent Catheters: a) DLP¿ Intracardiac Sump 20 Fr, Model Number 12012, b) DLP¿ Left Heart
| Recalling firm | Medtronic Perfusion Systems |
|---|---|
| Product | Medtronic Left Heart Vent Catheters: a) DLP¿ Intracardiac Sump 20 Fr, Model Number 12012, b) DLP¿ Left Heart Vent Catheter 10 Fr., Model Number 12008, c) DLP¿ Left Heart Vent Catheter 13 Fr., Model Number 12001, d) DLP¿ Left Heart Vent Catheter 13 Fr., Model Number 12113, e) DLP¿ Left Heart Vent Catheter 16 Fr., Model Number 12016, f) DLP¿ Left Heart Vent Catheter 20 Fr. Model Number 12002, g) DLP¿ Left Heart Vent Catheter 20 Fr. Model Number 12220, h) DLP¿ Pericardial Sump 38.1 cm (15 in), Model Number 12010, |
| Reason for recall | Potential for unsealed sterile packing. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Ongoing |
| Distribution | Worldwide distribution. |
| Recall initiated | 20240319 |
| Recall number | Z-1797-2024 |
| Category | device |
| State | MN |
| Country | United States |
$29/mo
Try RecallGuard →