FDA Device recall Z-2420-2015
Medtronic EOPA Arterial Cannula, Model # 77620
- FDA Device
- Class II
- terminated
- Published 2015-08-26
On 2015-08-26 the FDA classified a Class II recall of Medtronic EOPA Arterial Cannula, Model # 77620 by Medtronic Perfusion Systems, citing EOPA Arterial Cannula Devices in this lot were shipped without the guidewire.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2420-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-07-24 |
| Published | 2015-08-26 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Medtronic Perfusion Systems |
| Distribution | US |
Product
Medtronic EOPA Arterial Cannula, Model # 77620. Lot: 2015060544 intended to deliver oxygenated blood to the heart during cardiopulmonary bypass procedures for up to 6 hours in duration.
Reason
EOPA Arterial Cannula Devices in this lot were shipped without the guidewire.
Identifiers
| code_info | Lot number 2015060544; |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2420-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.