SilverGlide 6730160004Recalls & 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
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 04546540695796), received between Jan 8, 2025 and Jan 9, 2025 — classified as 3 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
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 9, 2025Flaked; Flaked
THE MANUFACTURER SERVICE TECHNICIAN REPORTED PIECES OF INSULATION WERE CHIPPED OFF THE TIP 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 21117785 ↗MalfunctionJan 8, 2025Flaked; Flaked
THE MANUFACTURER SERVICE TECHNICIAN REPORTED PIECES OF INSULATION WERE CHIPPED OFF THE TIP 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 21106674 ↗MalfunctionJan 8, 2025Flaked; Flaked
THE MANUFACTURER SERVICE TECHNICIAN REPORTED PIECES OF INSULATION WERE CHIPPED OFF THE TIP 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 21106509 ↗
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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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