FDAClass IIOctober 5, 2022

Product/Part: YelloPort Plus 5x70 Cannula + recall: Sterility Concern

Product/Part: YelloPort Plus 5x70 Cannula + Luer/YC0507001. For use in laparoscopic procedures.

Why was Product/Part: YelloPort Plus 5x70 Cannula + recalled?

Laparoscopic devices have a sterile symbol included on labels but devices are non-sterile.

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?

Part/UDI-DI/Lot: YC0507001/05051986001890/735652

Product
Product/Part: YelloPort Plus 5x70 Cannula + Luer/YC0507001. For use in laparoscopic procedures.
Recalling firm
Surgical Innovations Ltd
Quantity
1
Distribution
US: MA
Recall date
October 5, 2022
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls