PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: October 5, 2022 Initiated: January 20, 2022 #Z-1853-2022

Product Description

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

Reason for Recall

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

Details

Recalling Firm
Surgical Innovations Ltd
Units Affected
1
Distribution
US: MA
Location
Leeds, N/A

Frequently Asked Questions

What product was recalled?
Product/Part: YelloPort Plus 5x70 Cannula + Luer/YC0507001. For use in laparoscopic procedures.. Recalled by Surgical Innovations Ltd. Units affected: 1.
Why was this product recalled?
Laparoscopic devices have a sterile symbol included on labels but devices are non-sterile.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 5, 2022. Severity: Moderate. Recall number: Z-1853-2022.