Zimmer® Cannulated Screw System 00-1147-150-72Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00846468073329), received between Aug 14, 2025 and Aug 14, 2025 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).

1 other recall cover devices cleared under the same FDA submission (K003496); 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.

• InjuryAug 14, 2025Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED BY THE PATIENT'S LEGAL COUNSEL THAT THE PATIENT HAD A LEFT HEMIPELVIS ORIF ON (B)(6) 2018 WITH A ZIMMER RECON PLATE AND SYNTHES SCREWS. SUBSEQUENTLY, IT WAS REPORTED THAT AN UNSPECIFIED IMPLANT BROKE OR FAILED RESULTING IN PAINFUL FRAGMENTS IN THE PATIENT'S ABDOMEN. NO FURTHER INFORMATION HAS BEEN PROVIDED AT THIS TIME.

  Patient problems: Abdominal Pain

  MAUDE report 22809151 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K003496. One submission often covers many models, so check the product and lot details in each record.

• Z-0872-06 · Mar 3, 2006 · Terminated
  Zimmer Cannulated Screw System Cannulated Driver, 5.0 mm Hex, REF 1147-49-50; Catalog # 00-1147-049-50. Manufactured by Pioneer Surgical Technology, Marquette, MI; Distributed by