Euromi 1214L3GI-3350Recalls & reported problems
Euromi · The cannulas are reusable medical devices intended to be used by healthcare professionals for surgical or aesthetic applications. They are designed for the injection, irrigation, or aspiration of biological fluids, depending on their configuration. Manufactured from stainless steel or tungsten, they provide excellent mechanical and chemical resistance, ensuring durability and compatibility with standard cleaning, disinfection, and sterilization processes commonly used in the medical field. The cannulas are supplied non-sterile and must be thoroughly cleaned and sterilized before each use. They are available in various lengths, diameters, and tip configurations depending on the intended use, and are designed to ensure precise, safe, and comfortable handling. · Class 1
Data updated Oct 18, 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 03701416203319), received between Sep 28, 2026 and Sep 28, 2026 — 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
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.
MalfunctionSep 28, 2026Break
During a procedure, the cannula broke at the base during use. No clinical consequences were reported for the patient, and no injury, clinical signs or symptoms, additional medical intervention, hospitalization, prolonged procedure or permanent impairment were reported. The complaint was received on 15-Sep-2026. The affected device could not be returned for evaluation; photographs of the broken cannula were provided. The device was replaced under warranty.The event is being reported as a device malfunction because the breakage represents a failure of the device during use and, in accordance with the manufacturer's MDR assessment, the malfunction is considered reportable to FDA.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50912170 ↗
Other Cannula, Surgical, General & Plastic Surgery devices
- EXPEDIUM 279712580Medos International Sàrl · CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY69 reports
- AESCULAP MD610Aesculap, Inc. · CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY1 recall0 reports
- ENDOPATH TT012Ethicon Endo-Surgery, LLC · CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY47 reports
- NA 03.168.013Synthes GmbH · CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY37 reports
- NA 214120Medos International Sàrl · CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY28 reports
- Monoject 8881540111Cardinal Health, Inc. · CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY19 reports
- MOSS 279712500Depuy Spine, LLC · CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY12 reports
- Monoject 8881540133Cardinal Health, Inc. · CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY10 reports
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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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