SILVERGLIDE 6720190015Recalls & reported problems
Stryker Corporation · Non-Stick Bipolar Electrosurgical Precision Forceps Bayonet · 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 04546540532244), received between Nov 9, 2018 and Apr 24, 2019 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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
Device problems
- Detachment of Device or Device Component2
- Material Fragmentation2
Patient problems
- No Patient Involvement3
- No Information1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 24, 2019Detachment of Device or Device Component; Detachment of Device or Device Component
THE DEVICE GUIDE STOP WAS FOUND TO BE DISASSEMBLED FROM THE DEVICE, POSING THE RISK OF A SMALL COMPONENT BEING LOST IN A SURGICAL SITE, DURING CLEANING AT THE USER FACILITY. THERE WERE NO ADVERSE CONSEQUENCES RELATED TO THIS EVENT.
Patient problems: No Patient Involvement
MAUDE report 8545129 ↗MalfunctionDec 28, 2018Detachment of Device or Device Component; Detachment of Device or Device Component
THE DEVICE GUIDE STOP WAS FOUND TO BE DISASSEMBLED FROM THE DEVICE, POSING THE RISK OF A SMALL COMPONENT BEING LOST IN A SURGICAL SITE, DURING TESTING BY A MANUFACTURER SALES REPRESENTATIVE AT THE USER FACILITY. THERE WERE NO ADVERSE CONSEQUENCES RELATED TO THIS EVENT.
Patient problems: No Patient Involvement
MAUDE report 8202949 ↗MalfunctionDec 21, 2018Material Fragmentation; Material Fragmentation
THE DEVICE GUIDE STOP AND PIN WERE FOUND TO BE DISASSEMBLED FROM 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 8190991 ↗MalfunctionNov 9, 2018Material Fragmentation; Material Fragmentation
THE MANUFACTURER SALES REPRESENTATIVE STATED THE DEVICE INSULATION IS CHIPPING, POSING THE RISK OF A SMALL COMPONENT BEING LOST IN A SURGICAL SITE. ATTEMPTS ARE BEING MADE TO OBTAIN ADDITIONAL INFORMATION.
Patient problems: No Information
MAUDE report 8056649 ↗
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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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