Snapshot™ Fixation System 110019010Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887868251061), received between Jul 7, 2020 and Jul 7, 2020 — classified as 1 malfunction.

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

1 other recall cover devices cleared under the same FDA submission (K143037); 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.

• MalfunctionJul 7, 2020Packaging Problem; Packaging Problem

  IT WAS REPORTED THAT A SNAPSHOT MINI OPEN KIT WAS OPENED AND THE SEAL ON THE PACKAGE WAS STUCK TOGETHER CALLING INTO QUESTION ITS STERILITY.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10240231 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K143037. One submission often covers many models, so check the product and lot details in each record.

• Z-1009-2018 · Oct 25, 2017 · Terminated
  fastener, fixation, nondegradable, soft tissue