SonoLong Echo NanoLine® 531185-31ARecalls & reported problems
Pajunk GmbH Medizintechnologie · SonoLong Echo NanoLine® SonoLong NanoLine® cannula 19G x 50mm with facet 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 04048223126806), received between May 6, 2026 and May 6, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Material Rupture” (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
- Material Rupture1
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.
InjuryMay 6, 2026Material Rupture
(B)(4). THIS INCIDENT TOOK PLACE IN GERMANY. TENTITIVE TRANSLATION: THE CATHETER HAS REMAINED INSIDE THE PATIENT; THE SHEARED-OFF SECTION IS APPROXIMATELY 3-5 CM LONG. AN ULTRASOUND SCAN IS CURRENTLY BEING CARRIED OUT TO LOCATE IT, AND A MEDICAL DECISION WILL BE MADE REGARDING THE BEST COURSE OF ACTION FOR THE PATIENT.
Patient problems: Foreign Body In Patient
MAUDE report 25092267 ↗
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- BD Luer-Lok, BD Glaspak 405637Becton, Dickinson And Company · Anesthesia conduction kit1 recall7 reports
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- BD Glaspak 405675Becton, Dickinson And Company · Anesthesia conduction kit1 recall3 reports
- BD Luer-Lok, BD Glaspak 405609Becton, Dickinson And Company · Anesthesia conduction kit1 recall3 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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