CONMED GOLDLINERecalls & reported problems across all models
Conmed Corporation · 10 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 112
- Deaths reported
- 0
- Injuries reported
- 7
- Recalls
- 0
We found 10 models of CONMED GOLDLINE by Conmed Corporation in the FDA's device registry (GUDID). Together they are named in 112 adverse event reports in the FDA's MAUDE database, received between Oct 11, 2016 and Jun 11, 2026 — classified as 7 injuries, 105 malfunctions.
The most frequently reported specific device problem is “Delivered as Unsterile Product” (94 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 CONMED GOLDLINE problems
Device problems
- Delivered as Unsterile Product94
- Insufficient Device Problem Information6
- Self-Activation or Keying4
- Unsealed Device Packaging4
- Arcing1
- Device Packaging Compromised1
- Packaging Problem1
- Sparking1
Patient problems
- No Clinical Signs, Symptoms or Conditions94
- Burn(s)7
- No Patient Involvement4
- Not Applicable4
- Insufficient Information1
- No Consequences Or Impact To Patient1
- No Information1
- Superficial (First Degree) Burn1
CONMED GOLDLINE models
10 models, most reported first. Each model has its own page with its reports, recalls and device details.
- CONMED GOLDLINE 138114AELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES55 reports
- CONMED GOLDLINE 130309AELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES33 reports
- CONMED GOLDLINE 131309AELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES8 reports
- CONMED GOLDLINE 131307AELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES6 reports
- CONMED GOLDLINE 130307AELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES5 reports
- CONMED GOLDLINE 130318AElectrosurgical, cutting & coagulation & accessories1 report
- CONMED GOLDLINE 131318AElectrosurgical, cutting & coagulation & accessories1 report
- CONMED GOLDLINE 131319AElectrosurgical, cutting & coagulation & accessories1 report
- CONMED GOLDLINE 138659AELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- CONMED GOLDLINE 130326AELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
Recent CONMED GOLDLINE adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionJun 11, 2026Delivered as Unsterile Product
THIS DISTRIBUTOR REPORTED THAT THE 138114A DEVICE HAD AN INSUFFICIENT HEATSEAL FOUND DURING INCOMING INSPECTION. NO PATIENT INVOLVEMENT OCCURRED. THIS REPORT IS BEING RAISED DUE TO THE REPORTED MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25469244 ↗MalfunctionJun 9, 2026Delivered as Unsterile Product
THIS DISTRIBUTOR REPORTED THAT THE 138114A DEVICE HAD AN INSUFFICIENT HEATSEAL FOUND DURING INCOMING INSPECTION. NO PATIENT INVOLVEMENT OCCURRED. THIS REPORT IS BEING RAISED DUE TO THE REPORTED MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25443520 ↗MalfunctionJun 9, 2026Delivered as Unsterile Product
DURING INCOMING INSPECTION, THE DISTRIBUTOR REJECTED THIS DEVICE, 130309A, FOR AN INSUFFICIENT HEATSEAL. THERE WAS NO CONTACT WITH THE PATIENT AS THIS WAS FOUND DURING INCOMING INSPECTION. THIS WILL BE REPORTED AS A MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25442015 ↗MalfunctionJun 8, 2026Delivered as Unsterile Product
THE DISTRIBUTOR REPORTED THAT THE 138114A DEVICE HAD AN INSUFFICIENT HEATSEAL FOUND DURING INCOMING INSPECTION. NO PATIENT INVOLVEMENT OCCURRED. BASED ON THE INFORMATION AVAILABLE, AND THE DECISION TREE RESULTS, THIS COMPLAINT DOES MEET THE DEFINITION OF A REPORTABLE EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25432874 ↗MalfunctionMar 17, 2026Delivered as Unsterile Product
DURING INCOMING INSPECTION, THE DISTRIBUTOR REJECTED THIS DEVICE, 138114A, FOR AN INSUFFICIENT HEATSEAL. THERE WAS NO CONTACT WITH THE PATIENT AS THIS WAS FOUND DURING INCOMING INSPECTION. DUE TO THE POTENTIAL SEVERITY OF A BREACH IN STERILITY, THIS COMPLAINT MEETS THE CRITERIA FOR A REPORTABLE EVENT. THIS WILL BE REPORTED AS A MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24619786 ↗MalfunctionMar 12, 2026Delivered as Unsterile Product
DURING INCOMING INSPECTION, THE DISTRIBUTOR REJECTED THIS DEVICE, 138114A, FOR AN INSUFFICIENT HEATSEAL. THERE WAS NO CONTACT WITH THE PATIENT AS THIS WAS FOUND DURING INCOMING INSPECTION. THIS WILL BE REPORTED AS A MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24578529 ↗MalfunctionMar 12, 2026Delivered as Unsterile Product
DURING INCOMING INSPECTION, THE DISTRIBUTOR REJECTED THIS DEVICE, 138114A, FOR AN INSUFFICIENT HEATSEAL. THERE WAS NO CONTACT WITH THE PATIENT AS THIS WAS FOUND DURING INCOMING INSPECTION. THIS WILL BE REPORTED AS A MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24578525 ↗MalfunctionMar 10, 2026Delivered as Unsterile Product
DURING INCOMING INSPECTION, THE DISTRIBUTOR REJECTED THIS DEVICE, 138114A, FOR AN INSUFFICIENT HEATSEAL. THERE WAS NO CONTACT WITH THE PATIENT AS THIS WAS FOUND DURING INCOMING INSPECTION. THIS REPORT IS BEING RAISED DUE TO THE REPORTED MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24559724 ↗MalfunctionMar 10, 2026Delivered as Unsterile Product
THIS DISTRIBUTOR REPORTED THAT THE 138114A DEVICE HAD AN INSUFFICIENT HEATSEAL FOUND DURING INCOMING INSPECTION. NO PATIENT INVOLVEMENT OCCURRED. THIS REPORT IS BEING RAISED DUE TO THE REPORTED MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24559720 ↗MalfunctionMar 5, 2026Delivered as Unsterile Product
DURING INCOMING INSPECTION, THE DISTRIBUTOR REJECTED THIS DEVICE, 138114A, FOR AN INSUFFICIENT HEATSEAL. THERE WAS NO CONTACT WITH THE PATIENT AS THIS WAS FOUND DURING INCOMING INSPECTION. THIS REPORT IS BEING RAISED DUE TO THE REPORTED MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24518924 ↗MalfunctionDec 15, 2025Delivered as Unsterile Product; Delivered as Unsterile Product
THE DISTRIBUTOR REPORTED THAT THE 138114A DEVICE HAD AN INSUFFICIENT HEATSEAL FOUND DURING INCOMING INSPECTION. NO PATIENT INVOLVEMENT OCCURRED. THIS REPORT IS BEING RAISED DUE TO THE REPORTED MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23804499 ↗MalfunctionDec 15, 2025Delivered as Unsterile Product; Delivered as Unsterile Product
DURING INCOMING INSPECTION, THE DISTRIBUTOR REJECTED THIS DEVICE, 138114A, FOR AN INSUFFICIENT HEATSEAL. THERE WAS NO CONTACT WITH THE PATIENT AS THIS WAS FOUND DURING INCOMING INSPECTION. THIS WILL BE REPORTED AS A MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23803086 ↗MalfunctionDec 12, 2025Delivered as Unsterile Product; Delivered as Unsterile Product
THE DISTRIBUTOR REPORTED THAT THE 138114A DEVICE HAD AN INSUFFICIENT HEATSEAL FOUND DURING INCOMING INSPECTION. NO PATIENT INVOLVEMENT OCCURRED. THIS REPORT IS BEING RAISED DUE TO THE REPORTED MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23788100 ↗MalfunctionDec 11, 2025Delivered as Unsterile Product; Delivered as Unsterile Product
DURING INCOMING INSPECTION, THE DISTRIBUTOR REJECTED THIS DEVICE, 130309A, FOR AN INSUFFICIENT HEATSEAL. THERE WAS NO CONTACT WITH THE PATIENT AS THIS WAS FOUND DURING INCOMING INSPECTION. THIS WILL BE REPORTED AS A MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23779802 ↗MalfunctionDec 11, 2025Delivered as Unsterile Product; Delivered as Unsterile Product
THE DISTRIBUTOR REPORTED THAT THE 130309A DEVICE HAD AN INSUFFICIENT HEATSEAL FOUND DURING INCOMING INSPECTION. NO PATIENT INVOLVEMENT OCCURRED. THIS REPORT IS BEING RAISED DUE TO THE REPORTED MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23777147 ↗
Other Conmed Corporation products
All Conmed Corporation devices →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.
How reports and recalls are matched · Editorial policy · Report an error on this page