Osteotomy Compression Plates UOCP-SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00842188101533), received between Mar 22, 2018 and Mar 22, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Manufacturing, Packaging or Shipping Problem” (1 report).

1 other recall cover devices cleared under the same FDA submission (K043263); 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. How this data works · Data updated Oct 13, 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.

• MalfunctionMar 22, 2018Manufacturing, Packaging or Shipping Problem; Manufacturing, Packaging or Shipping Problem

  ON (B)(6) 2018, TRIMED WAS NOTIFIED THAT TWO HOLES, OF UOCP-S PLATE, THAT TAKE THE SAW GUIDE WERE ON THE WRONG SIDE OF THE PLATE. THE SURGEON WENT TO LEAVE THE PLATE IN-SITU, AS THE ISSUE ONLY CAME TO LIGHT ONCE THE OSTEOTOMY WAS PERFORMED. THE SURGEON USED A LAG SCREW THROUGH THE SLOTTED HOLE INSTEAD, THE OSTEOTOMY WAS STABLE. TRIMED WAS NOTIFIED BY A DISTRIBUTOR, (B)(4), IN (B)(6). THIS EVENT HAPPENED IN A CLINICAL SETTING, AND THIS IS THE FIRST EVENT OF ITS KIND FOR THE UOCP-S PLATE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7363139 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K043263. One submission often covers many models, so check the product and lot details in each record.

• Z-2877-2018 · Apr 16, 2018 · Terminated
  Ulnar Osteotomy Compression Plate, Short Model: UOCP-S Product Usage: The UOCP-S is provided non-sterile with the required fixation screws and surgical instrumentation. The TriMed