AESCULAP MF513RRecalls & reported problems
Aesculap, Inc. · FRAZIER Suction Tube, angled, 7", (180 mm), 7FR, non-sterile, reusable · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04046964573071), received between Jun 20, 2025 and Jun 20, 2025 — classified as 1 injury.
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.
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.
InjuryJun 20, 2025Break; Break
IT WAS REPORTED TO AESCULAP INC. THAT A FRAZIER SLOT SUCT TUBE ANG 7FR 180MM) PART # MF513R) WAS USED DURING AN ACDF C 4-5, 5-6, 6-7 SOMETIME IN (B)(6) 2024. ACCORDING TO THE COMPLAINANT THE DEVICE SUCTION BROKE AT WELD POINT WHERE SUCTION ATTACHES TO ADAPTER/LUER. REPORTEDLY THE PIECES WERE RETRIEVED AND AN X-RAY WAS PERFORMED TO CONFIRM ALL PIECES WERE REMOVED. A NEW SUCTION WAS OPENED AND USED TO COMPLETE THE PROCEDURE. A TEN-MINUTE DELAY TO THE PROCEDURE WAS ALSO REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22296729 ↗
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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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