YelloPort Plus - Laparoscopic Port Access System YC0515010Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 05051986001975), received between Nov 16, 2017 and Nov 24, 2017 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (2 reports).

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 24, 2017Break

  A DISTRIBUTOR REPORTED THAT A YELLOPORT PLUS CANNULA BROKE INSIDE A PATIENT DURING AN OPERATION.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7057401 ↗
• MalfunctionNov 16, 2017Break; Detachment Of Device Component

  A DISTRIBUTOR REPORTED AN INCIDENT THAT OCCURED AT A HOSPITAL ((B)(6)). DURING SURGERY, A SMALL PART FROM THE TIP OF A YELLOPORT CANNULA BROKE OFF.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7036505 ↗

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.