EpiLong Tuohy 0331152-51Recalls & reported problems
Pajunk GmbH Medizintechnologie · EpiLong · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 14048223012991), received between Jan 4, 2018 and Apr 11, 2019 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Blocked Connection” (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
- Blocked Connection1
- Device Misassembled During Manufacturing /Shipping1
- No Flow1
- Nonstandard Device1
- Product Quality Problem1
Patient problems
- Awareness During Anesthesia1
- No Consequences Or Impact To Patient1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 11, 2019Blocked Connection; Blocked Connection
(B)(6). TENTATIVE SUMMARIZING TRANSLATION FROM INITIAL REPORTER'S NARRATIVE: DISTAL END OF CATHETER IS CLOSED.
Patient problems: Awareness During Anesthesia
MAUDE report 8502929 ↗MalfunctionJan 4, 2018Nonstandard Device; Product Quality Problem; Device Misassembled During Manufacturing /Shipping; No Flow; Nonstandard Device; Product Quality Problem; Device Misassembled During Manufacturing /Shipping; No Flow
(B)(4). SUMMARIZING TRANSLATION FROM INITIAL REPORTER´S NARRATIVE: THE EPIDURAL CATHETER IS LACKING THE DISTAL CENTRAL OPENING. NO ANAESTHESIA CONDUCTION. CATHETER HAS TO BE REMOVED/ REPLACED. PROLOGUED INITIAL ANAESTHESIA PROCEDURE (APPROX. 15 MINUTES). NO ADVERSE OUTCOME FOR THE PATIENT.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 7163134 ↗
Other Anesthesia conduction kit devices
- BD Luer-Lok, BD Glaspak 405671Becton, Dickinson And Company · Anesthesia conduction kit1 recall68 reports
- ARROW IPN922678Teleflex Incorporated · Anesthesia conduction kit2 recalls0 reports
- 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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