Neptune E-SEP 0703-007-070Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327297812), received between Jul 13, 2023 and Jul 16, 2024 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Expiration Date Error” (1 report).

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.

• MalfunctionJul 16, 2024Expiration Date Error; Expiration Date Error

  IT WAS REPORTED THAT EXPIRED STRYKER PRODUCT WAS SHIPPED TO THE CUSTOMER. IT WAS ALSO REPORTED THAT THIS EVENT DID NOT OCCUR DURING A SURGICAL PROCEDURE, AND THERE WAS NO DELAY, NO MEDICAL INTERVENTION AND NO ADVERSE CONSEQUENCES AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19750265 ↗
• MalfunctionJul 13, 2023Fracture; Fracture

  IT WAS REPORTED VIA HEALTH CANADA: REFERENCE # 1041041: THAT THE LOOP T BAR ELECTRODE BROKE DURING A PROCEDURE. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITHOUT A CLINICALLY SIGNIFICANT DELAY; NO ADVERSE CONSEQUENCES OR MEDICAL INTERVENTION WERE REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17321811 ↗