YelloPort Plus - Laparoscopic Port Access System YC0509501Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05051986001388), received between Nov 27, 2017 and Nov 27, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (1 report).

1 other recall cover devices cleared under the same FDA submission (K070712); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 27, 2017Break; Detachment Of Device Component

  A DISTRIBUTOR REPORTED A COMPLAINT TO SURGICAL INNOVATIONS. THE COMPLAINT DETAILS STATE, DURING A LAPAROSCOPIC APPENDECTOMY SURGERY, A DOCTOR FOUND A BREAK ON TOP OF THE CANNULA (2 DEVICES AFFECTED) AFTER 30 MINUTES OF THE SURGERY. NO PATIENT HARM OR INJURY HAS BEEN REPORTED. A X-RAY AND CT SCAN WERE CARRIED OUT TO LOCATE THE MISSING PIECE HOWEVER NO PIECE WAS FOUND. THE DISTRIBUTOR HAS CONFIRMED THAT THERE WAS NO PATIENT HARM OR DEATH.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7058925 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K070712. One submission often covers many models, so check the product and lot details in each record.

• Z-1853-2022 · Jan 20, 2022 · Open, Classified
  Product/Part: YelloPort Plus 5x70 Cannula + Luer/YC0507001. For use in laparoscopic procedures.