No image published for this recall
The official notice did not include a photo. Check the product details and identifiers below.
No image published for this recall
EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model
Official notice
5 Aug 2026
Last checked
22 Sept 2026
An official FDA notice concerns Medtronic Perfusion. The notice reports an injury risk. Stop using the product and follow the official notice. Published 2026-08-05. Lots: 0232446429, 0232446444. Recall numbers: Z-2806-2026. Check the official notice for the complete list.
What to do now
Instructions for consumers are available in the official FDA notice.
Units affected
21,290
Recall number
Z-2806-2026
Official notice
2026-08-05
The hazard
The hazard
Injury risk
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Lots
Other
Event Ids
Recall Numbers
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Turn on recall alertsWhere it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand: Medtronic Perfusion. Contact: Medtronic Perfusion Systems.
Source & status
Source & status
Recall details
Recall details
Recall number
Event id
Units affected
Status
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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