SILVERGLIDERecalls & reported problems across all models
Stryker Corporation · 60 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 274
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 0
We found 60 models of SILVERGLIDE by Stryker Corporation in the FDA's device registry (GUDID). Together they are named in 274 adverse event reports in the FDA's MAUDE database, received between Jun 5, 2018 and Aug 4, 2025 — classified as 274 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (152 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported SILVERGLIDE problems
Device problems
- Detachment of Device or Device Component152
- Flaked110
- Material Fragmentation10
- Fracture1
- Material Split, Cut or Torn1
- Peeled/Delaminated1
Patient problems
- No Clinical Signs, Symptoms or Conditions192
- No Patient Involvement79
- Insufficient Information3
- No Consequences Or Impact To Patient3
- No Information2
- No Known Impact Or Consequence To Patient1
SILVERGLIDE models
60 models, most reported first. Each model has its own page with its reports, recalls and device details.
- SILVERGLIDE 6720220012ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES34 reports
- SILVERGLIDE 6720240012ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES24 reports
- SILVERGLIDE 6720220007ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES21 reports
- SILVERGLIDE 6720190007ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES18 reports
- SILVERGLIDE 6720220015ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES12 reports
- SILVERGLIDE 6720240007ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES12 reports
- SILVERGLIDE 6720190010ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES11 reports
- SilverGlide 6730220012ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES7 reports
- SilverGlide 6730240012ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES7 reports
- SILVERGLIDE 6710210007ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES7 reports
- SILVERGLIDE 6720190004ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES6 reports
- SilverGlide 6730240020ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES6 reports
- SilverGlide 6730240015ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES5 reports
- SILVERGLIDE 6710190010ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES5 reports
- SILVERGLIDE 6710190012ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES4 reports
- SILVERGLIDE 6715125007ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES4 reports
- SILVERGLIDE 6715125012ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES4 reports
- SILVERGLIDE 6720190015ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES4 reports
- SILVERGLIDE 6720220004ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES4 reports
- SILVERGLIDE 6720240004ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES4 reports
- SILVERGLIDE 6720240015ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES4 reports
- SilverGlide 6730220020ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES4 reports
- SILVERGLIDE 6710210012ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES4 reports
- SILVERGLIDE 6720220020ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES4 reports
- SILVERGLIDE 6750200004ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES3 reports
- SILVERGLIDE 6750250012ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES3 reports
- SilverGlide 6730160004ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES3 reports
- SilverGlide 6730220007ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES3 reports
- SilverGlide 6730220015ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES3 reports
- SilverGlide 6730220107ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES3 reports
- SILVERGLIDE 6710190007ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES2 reports
- SILVERGLIDE 6715150012ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES2 reports
- SILVERGLIDE 6750230015ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES2 reports
- SILVERGLIDE 6750250007ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES2 reports
- SilverGlide 6730190004ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES2 reports
- SilverGlide 6730190007ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES2 reports
- SilverGlide 6730190020ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES2 reports
- SilverGlide 6730240007ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES2 reports
- SILVERGLIDE 6710210020ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES2 reports
- SILVERGLIDE 6720190020ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES2 reports
- SILVERGLIDE 6720240020ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES2 reports
- SILVERGLIDE 6710190015ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- SILVERGLIDE 6715100004ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- SILVERGLIDE 6715100007ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- SILVERGLIDE 6720155004ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- SILVERGLIDE 6720155007ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- SILVERGLIDE 6720155015ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- SILVERGLIDE 6740190012ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- SILVERGLIDE 6750140007ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- SILVERGLIDE 6750200007ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- SILVERGLIDE 6750230007ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- SILVERGLIDE 6750250507ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- SILVERGLIDE 6750280012ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- SilverGlide 6730160007ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- SilverGlide 6730160010ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- SilverGlide 6730190012ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- SilverGlide 6730240507ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- SilverGlide 6730240607ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- SILVERGLIDE 6710210015ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- SILVERGLIDE 6740250012ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
Recent SILVERGLIDE adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionAug 4, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
THE MANUFACTURER SERVICE TECHNICIAN REPORTED ONE OF THE TIPS OF THE DEVICE WAS OBSERVED TO BE FRACTURED OFF AND MISSING DURING A SERVICE EVALUATION AT THE MANUFACTURER FACILITY. THERE WERE NO ADVERSE CONSEQUENCES RELATED TO THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22701455 ↗MalfunctionJul 23, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
THE USER FACILITY REPORTED ONE OF THE TIPS OF THE DEVICE WAS FRACTURED OFF AND MISSING DURING TESTING PRIOR TO A PROCEDURE. THERE WAS NO PATIENT INVOLVEMENT, NO MEDICAL INTERVENTION, AND NO ADVERSE CONSEQUENCES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22575609 ↗MalfunctionJul 23, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
THE GUIDE STOP AND ONE OF THE TIPS WERE FOUND TO BE DISASSEMBLED FROM THE DEVICE, POSING THE RISK OF A SMALL COMPONENT BEING LOST IN A SURGICAL SITE, DURING TESTING AT THE USER FACILITY. THERE WERE NO ADVERSE CONSEQUENCES RELATED TO THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22575608 ↗MalfunctionJul 17, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
THE MANUFACTURER SERVICE TECHNICIAN REPORTED ONE OF THE TIPS OF THE DEVICE WAS OBSERVED TO BE FRACTURED OFF AND MISSING DURING A SERVICE EVALUATION AT THE MANUFACTURER FACILITY. THERE WERE NO ADVERSE CONSEQUENCES RELATED TO THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22529750 ↗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 22493875 ↗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 ↗MalfunctionJul 9, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
THE MANUFACTURER SERVICE TECHNICIAN REPORTED THE GUIDE STOP WAS FRACTURED OFF AND MISSING FROM THE DEVICE DURING A SERVICE EVALUATION AT THE MANUFACTURER FACILITY. THERE WERE NO ADVERSE CONSEQUENCES RELATED TO THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22460775 ↗MalfunctionJul 9, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
THE MANUFACTURER SERVICE TECHNICIAN REPORTED THE GUIDE STOP WAS FRACTURED OFF AND MISSING FROM THE DEVICE DURING A SERVICE EVALUATION AT THE MANUFACTURER FACILITY. THERE WERE NO ADVERSE CONSEQUENCES RELATED TO THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22459272 ↗MalfunctionJul 9, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
THE MANUFACTURER SERVICE TECHNICIAN REPORTED THE GUIDE STOP WAS FRACTURED OFF AND MISSING FROM THE DEVICE DURING A SERVICE EVALUATION AT THE MANUFACTURER FACILITY. THERE WERE NO ADVERSE CONSEQUENCES RELATED TO THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22459259 ↗MalfunctionJul 7, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
THE MANUFACTURER SERVICE TECHNICIAN REPORTED ONE OF THE TIPS OF THE DEVICE WAS OBSERVED TO BE FRACTURED OFF AND MISSING DURING A SERVICE EVALUATION AT THE MANUFACTURER FACILITY. THERE WERE NO ADVERSE CONSEQUENCES RELATED TO THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22419916 ↗MalfunctionJul 7, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
THE MANUFACTURER SERVICE TECHNICIAN REPORTED THE GUIDE STOP WAS FRACTURED OFF AND MISSING FROM THE DEVICE DURING A SERVICE EVALUATION AT THE MANUFACTURER FACILITY. THERE WERE NO ADVERSE CONSEQUENCES RELATED TO THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22419900 ↗MalfunctionJul 7, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
THE MANUFACTURER SERVICE TECHNICIAN REPORTED ONE OF THE TIPS OF THE DEVICE WAS OBSERVED TO BE FRACTURED OFF AND MISSING DURING A SERVICE EVALUATION AT THE MANUFACTURER FACILITY. THERE WERE NO ADVERSE CONSEQUENCES RELATED TO THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22419869 ↗MalfunctionJul 7, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
THE MANUFACTURER SERVICE TECHNICIAN REPORTED ONE OF THE TIPS OF THE DEVICE WAS OBSERVED TO BE FRACTURED OFF AND MISSING DURING A SERVICE EVALUATION AT THE MANUFACTURER FACILITY. THERE WERE NO ADVERSE CONSEQUENCES RELATED TO THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22419858 ↗MalfunctionJul 7, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
THE MANUFACTURER SERVICE TECHNICIAN REPORTED THE GUIDE STOP WAS FRACTURED OFF AND MISSING FROM THE DEVICE DURING A SERVICE EVALUATION AT THE MANUFACTURER FACILITY. THERE WERE NO ADVERSE CONSEQUENCES RELATED TO THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22419816 ↗MalfunctionJun 30, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
THE MANUFACTURER SERVICE TECHNICIAN REPORTED ONE OF THE TIPS OF THE DEVICE WAS OBSERVED TO BE FRACTURED OFF AND MISSING DURING A SERVICE EVALUATION AT THE MANUFACTURER FACILITY. THERE WERE NO ADVERSE CONSEQUENCES RELATED TO THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22359637 ↗
Other Stryker Corporation products
- RemB7 models · 3,073 reports
- Prime Series21 models · 1,548 reports · 2 recalls
- TARGET114 models · 1,077 reports
- ProCuity17 models · 368 reports · 13 recalls
- Spetzler-Malis20 models · 7 reports · 19 recalls
- SYNCHRO 28 models · 313 reports · 9 recalls
- Neptune E-SEP19 models · 412 reports · 7 recalls
- StrykeFlow4 models · 552 reports · 4 recalls
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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