Skip to content

HOFFMANN 4933-1-712Recalls & reported problems

Stryker GmbH · Washer LRF (Blue) · Class 2 · Implant

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 07613252610557), received between Aug 31, 2023 and Aug 31, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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

  • Break1
  • Fracture1
  • Off-Label Use1

Patient problems

  • Failure of Implant1
  • Insufficient Information1

Recent adverse event reports

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

  • MalfunctionAug 31, 2023Break; Fracture; Off-Label Use; Break; Fracture; Off-Label Use

    NO EVENT TO REPORT AS OF YET, AWAITING FURTHER INFORMATION. UPDATE: "WIRE BREAKAGE".

    Patient problems: Failure of Implant; Insufficient Information

    MAUDE report 17666979 ↗

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.