CLEARFIX 253113Recalls & reported problems
Medos International Sàrl · CLEARFIX Calibration Tool Straight · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- 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 10886705012640), received between May 8, 2024 and May 8, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Use of Device Problem” (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.
Reports received per month
Most reported problems
Device problems
- Use of Device Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 8, 2024Use of Device Problem; Use of Device Problem
IT WAS REPORTED THAT PRIOR TO AN UNSPECIFIED SURGICAL PROCEDURE THE ARTHRO PUSHER/CUTTER, CLEARFIX CALIBR TOOL STR, CLEARFIX RASP STR UP 45 FACE, CLEARFIX RASP STR UP 90 FACE AND ARTHRO PUSHER/CUTTER DEVICES WERE BEING USED WHEN BOTH SUTURE CUTTER WAS BLUNT AND MALLEABLE ALL BENT NOT REUSABLE. MENISCUS RASP MISSING. THIS EVENT DID NOT OCCUR DURING SURGERY. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. NO ADDITIONAL INFORMATION WAS PROVIDED. THIS IS REPORT 2 OF 5 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19273146 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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