SILVERGLIDE 6720190020Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04546540714916), received between Feb 25, 2022 and Dec 16, 2022 — classified as 2 malfunctions.

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

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 16, 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.

• MalfunctionDec 16, 2022Flaked; Flaked

  IT WAS REPORTED THAT DURING EVALUATION AT THE MANUFACTURER FACILITY, THE DEVICE TIPS WERE FOUND TO BE CHIPPED AND SILVER PLATING MATERIAL WAS MISSING, POSING THE RISK OF MATERIAL BEING LOST IN A SURGICAL SITE. THERE WERE NO ADVERSE CONSEQUENCES RELATED TO THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15999731 ↗
• MalfunctionFeb 25, 2022Flaked; Flaked

  IT WAS REPORTED THAT DURING TESTING OF THE DEVICE AT THE USER FACILITY STERILE PROCESSING DEPARTMENT, THE DEVICE TIPS WERE FOUND TO BE CHIPPED AND SILVER PLATING MATERIAL WAS MISSING, POSING THE RISK OF A SMALL COMPONENT BEING LOST IN A SURGICAL SITE. THERE WERE NO ADVERSE CONSEQUENCES RELATED TO THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13604824 ↗