Medtronic EOPA Arterial Cannula — Class II medical device recall Z-2420-2015
Terminated recall by Medtronic Perfusion Systems, reported 2015-08-26, distributed nationwide. EOPA Arterial Cannula Devices in this lot were shipped without the guidewire.
| Recall number | Z-2420-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Perfusion Systems, Brooklyn Park, MN, United States |
| Recall initiated | 2015-07-24 |
| Classified | 2015-08-19 |
| Reported by FDA | 2015-08-26 |
| Terminated | 2016-04-04 |
| Distributed | Nationwide (US) |
| Countries outside the US | DE, HK, IT |
| Lot numbers | 2015060544 |
| Model numbers | 77620 |
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 for recall
EOPA Arterial Cannula Devices in this lot were shipped without the guidewire.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2420-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.