Ascension PIP PIP-200-20P-WWRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10381780000471), received between Jul 18, 2022 and Jul 18, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (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.

• InjuryJul 18, 2022Fracture; Fracture

  IT WAS REPORTED THAT, DURING A PIP TOTAL JOINT SURGERY, THE PIP SZ. 20 PROXIMAL SHEARED OFF WHEN IMPACTED GENTLY INTO THE PATIENT¿S MIDDLE PHALANGEAL BONE OF PATIENT LEFT RING FINGER. THE IMPLANT STEM WAS EMBEDDED IN THE PATIENT MEDULLARY CANAL AND IT WAS REMOVED USING A K WIRE DRILLED INTO THE MIDDLE PHALANX, PROXIMAL TO THE IMPLANT, BEFORE IMPLANTING A REPLACEMENT. SURGERY WAS RESUMED, AFTER A NON-SIGNIFICANT DELAY, WITH A BACK-UP DEVICE. NO FURTHER COMPLICATIONS WERE REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15048307 ↗