Implant Partners KPONTP32WDRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI M684KPONTP32WD1), received between Jul 19, 2022 and Jul 19, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Loss of Osseointegration” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryJul 19, 2022Loss of Osseointegration; Loss of Osseointegration

  ALLEGEDLY, CUSTOMER EXPERIENCE REPRESENTATIVE RECEIVED A CALL FROM A PATIENT'S RELATIVE INQUIRING ABOUT SOME IMPLANT PARTNERS PARTS THAT HAVE BEEN RECALLED AND SHE WANTED TO KNOW IF THE ITEMS USED ON HER BROTHER?S SURGERY SOME TIME AGO SHOULD BE RECALLED AND WHAT THE PROCESS WOULD BE. SHE MENTIONED THAT ONE OF THE LOT NUMBERS ON HER BROTHER'S MEDICAL RECORDS IS 1852119, BUT SHE SAYS THERE ARE MANY ITEMS ON THE RECORDS AND SHE WOULD LIKE TO CHECK THEM ALL. A FOLLOW-UP CALL REGARDING THIS CASE WAS RECEIVED ON (B)(6) 2022: THE ORIGINAL CONVERSATIONS NEVER MENTIONED COMPLICATIONS AND ONLY REQUESTED IF ANY PRODUCTS HAD BEEN RECALLED. HOWEVER, ON THIS FOLLOW-UP PHONE CALL, THE PATIENT INDICATED LOOSENING OF IMPLANTS. NO FURTHER DETAILS HAVE BEEN PROVIDED. IT HAS NOT BEEN INDICATED IF THE DEVICES HAVE BEEN REVISED YET.

  Patient problems: Insufficient Information

  MAUDE report 15051846 ↗