SonoLong Echo NanoLine 531185-31CRecalls & reported problems
Pajunk GmbH Medizintechnologie · SonoLong Echo NanoLine SonoLong NanoLine cannula 18G x 50mm with Tuohy tip and · Class 2
Data updated Oct 18, 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 14048223019716), received between Mar 27, 2019 and Mar 27, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (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.
Most reported problems
Device problems
- Material Split, Cut or Torn1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 27, 2019Material Split, Cut or Torn; Material Split, Cut or Torn
(B)(4). INITIAL REPORTERS NARRATIVE:AN EXTREMITY OF THE KT AROUND 13 CM IS STAYED IN THE BACK OF THE PATIENT DURING THE PUNCTION. THIS PUNCTION WAS DONE WITHOUT DIFFICULTY. THE KT HAS BEEN IMPLEMENTED TO REALIZE A SURGERY. HE HAS BEEN IMPOSSIBLE TO INJECT AT THE END OF THE SURGERY. IT WAS NOTICE THAT A BEND OF THE KT WAS PRESENT AT THE INITIAL PUNCTION. TO TRY TO REMOVE THIS KT BEND, THIS ONE IS BROKEN. AFTER ULTRASOUND SCAN CHECK, IT WAS IMPOSSIBLE TO FIND THE KT. THE HOSPITAL DECIDED TO LET THE KT AND THE PATIENT HAS BEEN INFORMED. AN ATTEMPTS TO LOCALIZE THE KT BY SCAN WILL BE DONE IN THE FUTURE.
Patient problems: Foreign Body In Patient
MAUDE report 8454706 ↗
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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 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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