PLEXOLONG 521156-31ARecalls & reported problems
Pajunk GmbH Medizintechnologie · 521156-31A · 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 04048223116869), received between Jul 7, 2025 and Jul 7, 2025 — 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
- 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.
MalfunctionJul 7, 2025Break; Break
#IRN: (B)(4) INCIDENT OCCURRED IN FRANCE: AN ANAESTHETIST PLACED AN INJECTION CATHETER PREOPERATIVELY FOR ANALGESIA AFTER KNEE PROSTHESIS. THE CATHETER WAS INSERTED WITHOUT ANY PARTICULAR PROBLEM, BUT DURING INJECTION, IT BENT AND BROKE INSIDE THE PATIENT. THE SURGEON IN CHARGE OF THE KNEE REPLACEMENT HAD TO MAKE AN INCISION IN THE PATIENT'S THIGH IN ORDER TO RECOVER THE BROKEN END.
Patient problems: Foreign Body In Patient
MAUDE report 22412898 ↗
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- BD Luer-Lok, BD Glaspak 405707Becton, Dickinson And Company · Anesthesia conduction kit1 recall4 reports
- BD Luer-Lok, BD Glaspak 405609Becton, Dickinson And Company · Anesthesia conduction kit1 recall3 reports
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.