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HOFFMANN 4922-2-160Recalls & reported problems

Stryker GmbH · Post; 90 degree angled · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04546540681041), received between Feb 18, 2020 and Feb 18, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Difficult to Setup or Prepare” (1 report).

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

Device problems

  • Device Difficult to Setup or Prepare1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionFeb 18, 2020Device Difficult to Setup or Prepare; Device Difficult to Setup or Prepare

    THE ATTACHMENTS COULD NOT BE ATTACHED. REPLACEMENT DEVICES WERE AVAILABLE. ADDITIONALLY REPORTED: THE ATTACHMENT COULD NOT BE PUT INTO THE 5-HOLE PIN HOLDER. THE APPROACHES DID NOT FIT INTO THE "STAR BORE" PROVIDED FOR THEM. THE ORIGINAL H3 7MM T-WRENCHES TO LOOSEN THE SCREWS DURING TESTING WERE USED. THE CUSTOMER NOTICED THE PROBLEMS ALREADY WHEN CONNECTING THE PIN HOLDER WITH THE ATTACHMENTS, SO NO FURTHER ASSEMBLY WAS MADE.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9721700 ↗

Other APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT devices

All APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.