RAPIDLOC PANACRYL 228320Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886705010219), received between Sep 11, 2019 and Sep 11, 2019 — classified as 1 malfunction.

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 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.

• MalfunctionSep 11, 2019Material Deformation; Material Deformation

  THE SALES REP REPORTED VIA PHONE THAT THE TOP HAT ON THE CUSTOMER'S RAPIDLOC IMPLANT WAS BENT WHEN TAKING IT OUT OF THE PACKAGE PRIOR TO A KNEE SCOPE. NOT LIKELY TO RESULT IN PATIENT HARM OR THE NEED FOR ADDITIONAL MEDICAL OR SURGICAL INTERVENTION. THERE WERE NO PATIENT CONSEQUENCES OR DELAYS. THIS IS REPORT 1 FOR 1 (B)(4).

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8991688 ↗