Symmetry Olsen 90-8012Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00841785110405), received between Jan 4, 2023 and Jan 4, 2023 — classified as 1 malfunction.

1 other recall cover devices cleared under the same FDA submission (K982705); 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.

• MalfunctionJan 4, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE CUSTOMER ALLEGED THAT THEY ARE RECEIVING COMPLAINTS FROM OUR NEUROSURGEONS REGARDING THE NON-STICK BIPOLAR FORCEPS GETTING STUCK IN THE BRAIN TUMOR TISSUE DURING SURGERY, LEADING TO THE USE OF MICRO SCISSORS TO SEPERATE THE TISSUE FROM THE BIPOLAR. THERE HAS BEEN NO PATIENT HARM.

  Patient problems: Insufficient Information

  MAUDE report 16099369 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K982705. One submission often covers many models, so check the product and lot details in each record.

• Z-1995-2012 · Jun 1, 2012 · Terminated
  Bayonet Forceps 8.5" (215.9mm) Serrated 1.0 mm Tips Electrosurgical/Monopolar Forceps/Reusable, Model #41604, 510 (k) #K885199. The surgical device is package in non-sterile small