Symmetry Olsen 50-2111Recalls & reported problems
Aspen Surgical Products, Inc. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00841785107665), received between Aug 21, 2018 and Jan 30, 2020 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fire” (2 reports).
2 other recalls cover devices cleared under the same FDA submission (K111262); they may or may not involve this specific model.
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 18, 2026.
Most reported problems
Device problems
- Fire2
Patient problems
- No Consequences Or Impact To Patient1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 30, 2020Fire
THE MONOPOLAR CORD QUIT WORKING DURING THE CASE. THE TECH IN THE ROOM ADJUSTED THE CORD CONNECTION AND IT STARTED WORKING AGAIN BUT A SMALL FLAME ROSE FROM THE CORD NEAR THE MONOPOLAR SCISSOR CONNECTION. IT WENT OUT IMMEDIATELY WITH NO HARM TO THE PATIENT OR USER. THE EQUIPMENT WAS REMOVED FROM THE FILED AND NEW EQUIPMENT WAS USED TO COMPLETE THE CASE WITH NO OTHER ISSUES.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9648540 ↗MalfunctionAug 21, 2018Fire
OLSEN MONOPOLAR CORD CAUGHT ON FIRE. NO PATIENT OR STAFF INJURY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7803602 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K111262. One submission often covers many models, so check the product and lot details in each record.
- Z-1943-2018 · May 11, 2018 · TerminatedSymmetry Olsen monopolar cord: (a) Monopolar Cord, 1/8" Diameter Pin, TUR Connector, 10' (3.0m), REF 92002, QTY 50 (b) Monopolar Cord, Bovie to 90o Female Pin, 10' (3.0m), REF 40
- Z-1942-2018 · May 11, 2018 · TerminatedSymmetry Olsen bipolar cord: (a) Bipolar Cord, Twin Pin Connector to Shrouded Instrument Connector, 12' (3.6m), REF 87500, QTY 50 (b) Bipolar Cord, Twin Pin Connector, 12' (3.6m),
Other Electrosurgical, Cutting & Coagulation & Accessories devices
- Vasoview Hemopro 2 VH-4000Maquet Cardiovascular LLC · Electrosurgical, Cutting & Coagulation & Accessories6 recalls1 death3,232 reports
- LigaSure LF1937Covidien LP · Electrosurgical, cutting & coagulation & accessories3 deaths2,090 reports
- Olympus WB91051WOLYMPUS Winter & Ibe GmbH · Electrosurgical, Cutting & Coagulation & Accessories1 death1,951 reports
- Valleylab FT10 VLFT10GENCovidien LP · Electrosurgical, cutting & coagulation & accessories1 recall5 deaths1,062 reports
- LigaSure LF1837Covidien LP · ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 recall967 reports
- LigaSure LF2019Covidien LP · Electrosurgical, cutting & coagulation & accessories948 reports
- VAPR 225028Depuy Mitek, LLC · ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES895 reports
- LigaSure LF1923Covidien LP · Electrosurgical, cutting & coagulation & accessories855 reports
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 18, 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