Ascension® MCP MCP10030PWWRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10381780000419), received between Jul 7, 2022 and Jul 7, 2022 — classified as 1 injury.

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

1 other recall cover devices cleared under the same FDA submission (P000057); they may or may not involve this specific model.

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 7, 2022Fracture; Fracture

  IT WAS REPORTED THAT, DURING A MCP JOINT REPLACEMENT SURGERY, THE MCP SZ. 30 PROXIMAL WW WAS PUT IN AND, WHEN THE FINAL X-RAYS WHERE TOOK, THE TIP OF THE STEM WAS BROKEN OFF. THE STEM WAS RETRIEVED AND THE BROKEN TIP WAS DRILLED, A 2.7 MM SCREW WAS PLACED AND A PAIR OF PLIERS WERE ATTACHED TO THE SCREW AND THE TIP WAS HAMMERED OUT. SURGERY WAS RESUMED, AFTER A NON-SIGNIFICANT SURGICAL DELAY, WITH A BACK-UP 40 STEM. NO FURTHER COMPLICATIONS WERE REPORTED.

  Patient problems: Failure of Implant

  MAUDE report 14946834 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under P000057. One submission often covers many models, so check the product and lot details in each record.

• Z-0550-03 · Oct 31, 2002 · Terminated
  Ascension MCP, Prosthesis, Finger Joint, Metacarpophalangeal