EOPA Arterial Cannula recall: Labeling Error
EOPA Arterial Cannula, Model Numbers 77422 (22 Fr) and 77418 (18 Fr)
Why was EOPA Arterial Cannula recalled?
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Model 77418 UDI-DI: 20763000135618, Lot Numbers: 2022041038; Model 77422 UDI-DI: 20643169485970, Lot Number: 2023020934
- Product
- EOPA Arterial Cannula, Model Numbers 77422 (22 Fr) and 77418 (18 Fr)
- Recalling firm
- Medtronic Perfusion Systems
- Quantity
- 930 units
- Distribution
- Worldwide - US Nationwide distribution.
- Recall date
- January 29, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)