MotoCLIP™ 1442-1515Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00850310006090), received between Nov 1, 2016 and Nov 1, 2016 — classified as 1 injury.

The most frequently reported specific device problem is “Crack” (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.

• InjuryNov 1, 2016Crack; Failure to Align

  A 15MM MOTOCLIP WAS USED TO FIXATE AN AUSTIN BUNIONECTOMY. ONE LEG OF THE MOTOCLIP WAS ALLEGEDLY CUT TO SHORTEN THE LENGTH OF THE LEG. UPON INSERTION OF THE CLIP, SUPPOSEDLY THE LEGS DID NOT APPEAR TO LINE UP CORRECTLY WITH THE PRE DRILLED HOLES IN THE BONE. A MALLET WAS USED TO FULLY INSERT THE CLIP INTO THE PREPARED HOLES. UPON REMOVAL OF THE INSERTER, IT WAS NOTICED THAT THE BONE CORTEX WAS CRACKED DORSALLY. NO X-RAYS HAVE BEEN PROVIDED. A K-WIRE(S) WAS USED TO ADDRESS THE CRACKED CORTEX..

  Patient problems: No Information

  MAUDE report 6070286 ↗

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.