SilverGlide 6730240015Recalls & reported problems
Stryker Corporation · ProSeries Non-stick Bipolar Electrosurgical Forceps Bayonet Tip · Class 2
All models of SILVERGLIDE (60)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 04546540696076), received between Apr 24, 2019 and Jan 21, 2025 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Flaked” (5 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
- Flaked5
Patient problems
- No Patient Involvement3
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 21, 2025Flaked; Flaked
IT WAS REPORTED THAT DURING TESTING AT THE USER FACILITY, THE DEVICE INSULATION WAS FOUND TO BE WORN 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 21199035 ↗MalfunctionJan 21, 2025Flaked; Flaked
IT WAS REPORTED THAT DURING TESTING AT THE USER FACILITY, THE DEVICE INSULATION WAS FOUND TO BE WORN 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 21199032 ↗MalfunctionJun 4, 2019Flaked; Flaked
IT WAS REPORTED THAT DURING TESTING AT THE MANUFACTURER FACILITY INSULATION WAS CHIPPED OFF AND MISSINGFROM THE DEVICE, 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 Patient Involvement
MAUDE report 8668137 ↗MalfunctionApr 24, 2019Flaked; Flaked
IT WAS REPORTED THAT DURING CLEANING AT THE USER FACILITY, PIECES OF INSULATION WERE FOUND TO BE MISSING FROM 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 Patient Involvement
MAUDE report 8544458 ↗MalfunctionApr 24, 2019Flaked; Flaked
IT WAS REPORTED THAT DURING CLEANING AT THE USER FACILITY, PIECES OF INSULATION WERE FOUND TO BE MISSING FROM 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 Patient Involvement
MAUDE report 8544454 ↗
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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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