NA 242585Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10886705028795), received between Jul 7, 2020 and Jul 8, 2020 — classified as 2 injuries.

The most frequently reported specific device problem is “Material Deformation” (1 report).

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 16, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJul 8, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED BY SALES REP IN (B)(6) THAT DURING A KNEE ARTHROSCOPY, AN OBT CONCL,2.4,75,CW_STORZ WAS TOO SHARP AND DAMAGED THE CARTILAGE WHILE ENTERING THE KNEE. NO SURGICAL DELAY WAS REPORTED. THE PROCEDURE WAS COMPLETED USING THE SAME DEVICE. THERE WERE NO ADVERSE PATIENT CONSEQUENCES REPORTED. NO ADDITIONAL INFORMATION COULD BE PROVIDED.

  Patient problems: Tissue Damage

  MAUDE report 10246441 ↗
• InjuryJul 7, 2020Material Deformation; Material Deformation

  IT WAS REPORTED BY THE AFFILIATE IN (B)(6) THAT DURING A KNEE ARTHROSCOPY PROCEDURE, IT WAS OBSERVED THAT THE OBT_CONCL_4.0,175_CW_STORZ WAS TOO SHARP. THERE WAS NO DELAY THE SURGERY. ANOTHER LIKE DEVICE WAS USED TO COMPLETE THE SURGERY SUCCESSFULLY. THERE WAS DAMAGE TO PATIENT'S CARTILAGE. THERE WERE NO FRAGMENTS GENERATED AND THERE WERE NO PATIENT CONSEQUENCES. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: Tissue Damage

  MAUDE report 10240600 ↗