Symmetry Olsen 90020Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00841785110061), received between Nov 2, 2020 and Nov 2, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Burst Container or Vessel” (1 report).

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

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 2, 2020Burst Container or Vessel

  THE CUSTOMER ALLEGED THAT DURING THE MIDDLE OF THE SURGERY, THE CABLE BURST.

  Patient problems: Insufficient Information

  MAUDE report 10775061 ↗

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 · Terminated
  Symmetry 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 · Terminated
  Symmetry 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),