SILVERGLIDE 6710190012Recalls & reported problems
Stryker Corporation · Non-Stick Bipolar Electrosurgical Standard Forceps Cushing · Class 2
All models of SILVERGLIDE (60)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 04546540532084), received between Mar 22, 2019 and Jul 14, 2025 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Flaked” (3 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.
Reports received per month
Most reported problems
Device problems
- Flaked3
- Detachment of Device or Device Component1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- No Patient Involvement1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 14, 2025Flaked; Flaked
THE MANUFACTURER SERVICE TECHNICIAN REPORTED THE SILVER COATING WAS FLAKED OFF BOTH TIPS OF THE DEVICE, 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 22493451 ↗MalfunctionNov 28, 2023Flaked; Flaked
IT WAS REPORTED THAT DURING TESTING AT THE USER FACILITY, THE DEVICE INSULATION WAS FOUND TO BE COMING OFF THE DEVICE, POSING THE RISK OF A 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 18221033 ↗MalfunctionApr 25, 2023Flaked; Flaked
IT WAS REPORTED THAT DURING EVALUATION AT THE MANUFACTURER FACILITY, ONE DEVICE TIP WAS FOUND TO HAVE SILVER PLATING MATERIAL 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 16809046 ↗MalfunctionMar 22, 2019Detachment of Device or Device Component; Detachment of Device or Device Component
THE DEVICE WAS FOUND TO BE FRACTURED OFF THE DEVICE, POSING THE RISK OF A SMALL COMPONENT BEING LOST IN A SURGICAL SITE, DURING A SERVICE EVALUATION AT THE MANUFACTURER FACILITY. THERE WERE NO ADVERSE CONSEQUENCES RELATED TO THIS EVENT.
Patient problems: No Patient Involvement
MAUDE report 8446187 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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