QUICKANCHOR ORTHOCORD 222979Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886705008575), received between Mar 7, 2019 and Mar 7, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Entrapment of Device” (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 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.

• InjuryMar 7, 2019Entrapment of Device; Entrapment of Device

  IT WAS REPORTED BY THE AFFILIATE VIA EMAIL THAT DURING A ROTATOR CUFF REPAIR THE WIRE GOT STUCK AND HAD TO BE REPLACED BY A NEW ANCHOR. THE ANCHOR WAS LEFT IN THE PATIENT. THE PROCEDURE WAS COMPLETED BY MAKING A NEW HOLE AND USING A SECOND ANCHOR. ADDITIONAL INFORMATION PROVIDED BY THE AFFILIATE ON 02/26/2019 REPORTS THAT THERE IS NO ADDITIONAL INFORMATION PERTAINING TO PATIENT BONE QUALITY, IMPLANT CONDITION, OR SURGICAL TECHNIQUE. THE AFFILIATE DID REPORT THAT THERE WAS A MINUTE DELAY TO OBTAIN A NEW ANCHOR. IT WAS ALSO REPORTED THAT THE DEVICE WOULD NOT BE RETURNING BECAUSE IT IS STILL IMPLANTED IN THE PATIENT AND THERE WERE NO KNOWN CONSEQUENCES OR IMPACT TO THE PATIENT.

  Patient problems: Foreign Body In Patient; Injury; Not Applicable

  MAUDE report 8401716 ↗