EPILONG 0431157-51Recalls & reported problems
Pajunk GmbH Medizintechnologie · 0431157-51 · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 04048223115152), received between Sep 19, 2024 and Sep 19, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Complete Blockage” (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
- Complete Blockage1
- Material Separation1
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.
MalfunctionSep 19, 2024Complete Blockage; Material Separation; Complete Blockage; Material Separation
IRN# (B)(4). INCIDENT OCCURRED IN FRANCE: ORIGINAL TEXT: PATIENT OPÉRÉ LE 05/09 AVEC MISE EN PLACE D'UNE PÉRIDURAL LE JOUR MÊME SANS DIFFICULTÉ. EN SALLE DE SURVEILLANCE, L'EXTRÉMITÉ DU CATHÉTER DE PÉRIDURALE PARAIT DÉNUDÉ AVEC UNE PARTIE MÉTALLIQUE QUI PARAIT DISTENDUE. LE CATHÉTER EST COUPÉ POUR REMETTRE EN PLACE UN NOUVEAU FILTRE AVEC UNE ANALGÉSIE PÉRIDURALE FONCTIONNELLE PAR LA SUITE. RISQUE PATIENT: MAJORATION DU RISQUE INFECTIEUX ET RISQUE D'INEFFICACITÉ DE LA PÉRIDURALE. TRANSLATION: PATIENT OPERATED ON 05/09 WITH EPIDURAL INSERTED THE SAME DAY WITHOUT DIFFICULTY. IN THE MONITORING ROOM, THE TIP OF THE CATHETER APPEARED BARE, WITH A METAL PART THAT APPEARED DISTENDED. THE CATHETER IS CUT AND A NEW FILTER PUT IN PLACE, WITH FUNCTIONAL EPIDURAL ANALGESIA THERE AFTER. PATIENT RISK: INCREASED RISK OF INFECTION AND EPIDURAL INEFFECTIVENESS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20257204 ↗
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- BD Luer-Lok, BD Glaspak 405672Becton, Dickinson And Company · Anesthesia conduction kit1 recall27 reports
- BD Luer-Lok, BD Glaspak 405673Becton, Dickinson And Company · Anesthesia conduction kit1 recall10 reports
- BD Luer-Lok, BD Glaspak 405637Becton, Dickinson And Company · Anesthesia conduction kit1 recall7 reports
- BD Luer-Lok, BD Glaspak 405707Becton, Dickinson And Company · Anesthesia conduction kit1 recall4 reports
- 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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