Osteotomy Compression Plates UOCPRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00842188101526), received between Apr 24, 2026 and Apr 24, 2026 — classified as 1 malfunction.

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.

• MalfunctionApr 24, 2026Adverse Event Without Identified Device or Use Problem

  REGIONAL SALES MANAGER REPORTED ON (B)(6) 2026 THAT A SURGEON ENCOUNTERED THE PLATE 'LIFTING' FROM THE BONE AFTER HIS OVER-COMPRESSION AND BELIEVES IT MAY HAVE LED TO OVER SHORTENING. THE SURGEON MENTIONED THE SCRUB TECH BELIEVED THE ISSUE WAS DOING A QUARTER TURN LOOSENING IN THIS CASE MIGHT HAVE BEEN TOO MUCH WHICH ALLOWED THE COMPRESSION TO SLIDE UP UNDER THE PLATE AND PULLED THE PLATE AWAY A LITTLE BIT WHICH IS ALLOWING THE OVER SHORTENING. THE SURGEON AGREED THAT THIS WAS THE CAUSE AND SAID EVEN WHEN USING THE CLAMP, IT WOULD NOT NECESSARILY PREVENT LIFT OFF PROXIMATELY ONCE ITS COMPRESSED STATING HE HAD VERY GOOD APPOSITION AND NO SIDE-TO-SIDE TRANSLATION. THE SURGEON IS THINKING LOOSENING MAYBE ONLY AN EIGHT OF A TURN WILL HELP ALLEVIATE THE ISSUE IN FUTURE CASES. THE SURGEON STATED THERE WAS NO HARDWARE MALFUNCTION AND NO ADVERSE PATIENT AFFECT IN THEORY, HOWEVER, WITH OVER SHORTENING HE WON'T KNOW THE EFFECT UNTIL THE PATIENT IS FINISHED HEALING.

  Patient problems: Unspecified Musculoskeletal problem

  MAUDE report 24987661 ↗

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