SonoPlex Stim cannula Facet tip S 001187-77Recalls & reported problems
Pajunk GmbH Medizintechnologie · SonoPlex Stim cannula Facet tip S 21G (0,80) x 100mm, with injection tube and connecting cable · 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 14048223020606), received between Aug 23, 2018 and Aug 23, 2018 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (2 reports).
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
- Fluid/Blood Leak2
- Leak/Splash1
Patient problems
- No Patient Involvement2
- 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.
MalfunctionAug 23, 2018Fluid/Blood Leak; Leak/Splash; Fluid/Blood Leak
IRN# 579_292-18. ASPIRATION OF AIR LEAKAGE OF ANESTHETICS. LOT 1251, LOT 1252, LOT 1220.
Patient problems: No Known Impact Or Consequence To Patient; No Patient Involvement
MAUDE report 7808168 ↗MalfunctionAug 23, 2018Fluid/Blood Leak; Fluid/Blood Leak
(B)(4). WE HAVE RECEIVED 2 BOXES OR MORE OF DEFECTIVE NEEDLES. THEY ARE LEAKING BEFORE USE. IT IS ONLY PRODUCT # 001187-77 AND LOT #1251 PURCHASED ON (B)(4). ALL OTHER LOT #'S SEEM TO BE OKAY HOWEVER WE STILL NEED TO FILE A REPORT AND GET MORE NEEDLES IN. AS PREVIOUSLY STATED I HAVE 2 DEFECTIVE BOXES ON MY DESK (ONE BOX IS OPEN). CAN I BE CREDITED THESE? I PLACED AN ORDER FOR 2 NEW BOXES ON (B)(4).
Patient problems: No Patient Involvement
MAUDE report 7808033 ↗
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- ARROW IPN922605Teleflex Incorporated · NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)1 recall0 reports
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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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