MotoCLIP™ 1442-1010Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00850310006083), received between Sep 29, 2022 and Sep 29, 2022 — classified as 1 malfunction.

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

1 other recall cover devices cleared under the same FDA submission (K142727); 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.

• MalfunctionSep 29, 2022Fracture; Fracture

  WHILE THE NURSE WAS ATTEMPTING TO LOAD THE IMPLANT ONTO THE INSERTER SHE HAD DIFFICULTY DOING SO AND THE REP FELT AS IF THE LEGS OF THE INSERTER MIGHT HAVE BEEN BENT OR WEAKENED IN THE PROCESS. AFTER MENTIONING THIS TO THE DOCTOR, THE DOCTOR TESTED THE LEGS OF THE INSERTER WHILE THE IMPLANT WAS LOADED AND ONE LEG OF THE INSERTER IMMEDIATELY BROKE WITH EASE. THE BROKEN PIECES WERE DISCARDED AND ANOTHER KIT WAS OPENED AND SUCCESSFULLY USED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15501764 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K142727. One submission often covers many models, so check the product and lot details in each record.

• Z-1487-2017 · Feb 16, 2017 · Terminated
  MotoCLIP(TM) Super Elastic Fusion System, Size 18mm x 14mm x 14mm, REF 1442-1814, Rx Only, STERILE R.