YelloPort Plus - Laparoscopic Port Access System YC0507011Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05051986001364), received between Mar 9, 2020 and Mar 9, 2020 — classified as 1 injury.

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.

• InjuryMar 9, 2020Break; Component Missing

  THE CONCERNED PRODUCT WAS USED DURING PROCEDURE OF ABDOMINAL WALL SCAR HERNIA ON NOVEMBER 6TH, WEDNESDAY, WITHOUT ANY ISSUE. HOWEVER, THEY REALIZED THAT DISTAL END OF THE CANNULA WAS BROKEN AND MISSING WHEN THEY VISUALLY INSPECTED THE PRODUCT AFTER STERILIZATION. THEY WATCHED RECORDED VIDEO IN ORDER TO FIND THE MISSING PART AND CONFIRMED IT WAS DROPPED INSIDE THE PATIENT DURING PROCEDURE. TO RETRIEVE THE MISSING PART, SECOND LAPAROSCOPIC OPERATION WAS MADE. SINCE THE MISSING PART WAS DIFFICULT TO FIND, THEY SWITCHED THE OPERATION TO OPEN SURGERY AND MADE 10CM SURGICAL INCISION WAS MADE IN THE WALL OF THE ABDOMEN.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9806060 ↗

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.