Valleylab E2780-28Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884524000541), received between Dec 17, 2019 and Dec 17, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).

1 other recall cover devices cleared under the same FDA submission (K964175); 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. How this data works · Data updated Oct 13, 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.

• InjuryDec 17, 2019Detachment of Device or Device Component; Material Twisted/Bent; Detachment of Device or Device Component; Material Twisted/Bent

  ACCORDING TO THE REPORTER, DURING A LAPAROSCOPIC CHOLECYSTECTOMY PROCEDURE, THE DEVICE METAL TIP WAS BENT. LATER DURING FURTHER CAUTERIZATION THE METAL SPATULA TIP WAS NO LONGER PRESENT. ATTEMPTS TO RETRIEVE WERE UNSUCCESSFUL.

  Patient problems: Device Embedded In Tissue or Plaque

  MAUDE report 9482980 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K964175. One submission often covers many models, so check the product and lot details in each record.

• Z-1836-2017 · Jan 26, 2017 · Terminated
  Valleylab Laparoscopic Handset; Material # E2750; Laproscopic Handset Non-Sterile Bulk; Material # E2750NSB Product Usage: For use in 5mm cannulas or larger cannulas with 5mm ada