SonoTAP 1185-3E080Recalls & reported problems
Pajunk GmbH Medizintechnologie · SonoTAP 22G x 80mm with bevel tip and Cornerstone Reflectors · 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 14048223019761), received between Dec 13, 2017 and Dec 13, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “No Flow” (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
- No Flow1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 13, 2017No Flow; No Flow
(B)(4). INITIAL REPORTER´S NARRATIVE: NEEDLE IS BLOCKED PRIOR TO USE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7111801 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.