V. Mueller U-0572Recalls & reported problems
Steris Corporation · V. Mueller Neuro/Spine CHROMA-LINE BRAND TAKA inchesL inches SUCTION TUBE, STRAIGHT 12 FR, ORANGE WORKING LENGTH 5-1/2 inches 14CM · 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 10885403138317), received between Jul 2, 2024 and Jul 2, 2024 — 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.
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.
MalfunctionJul 2, 2024Break; Break
THE USER FACILITY REPORTED VIA MEDWATCH MW5155061 THAT, "TWO PIECES OF TAKA SUCTION CAME APART WHILE IN USE, BOTH RETRIEVED, NO HARM TO PATIENT." NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19654688 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.