Select Series Angled Tip Arterial Cannula recall: Labeling Error
Select Series Angled Tip Arterial Cannula, Model Number 72422 (22 Fr)
Why was Select Series Angled Tip 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 72422 UDI-DI: 20643169485970, Lot Numbers: 2023071075, 202309C075
- Product
- Select Series Angled Tip Arterial Cannula, Model Number 72422 (22 Fr)
- Recalling firm
- Medtronic Perfusion Systems
- Quantity
- 440 units
- Distribution
- Worldwide - US Nationwide distribution.
- Recall date
- January 29, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)