UniPlex NanoLine 001156-74Recalls & reported problems
Pajunk GmbH Medizintechnologie · UniPlex NanoLine UP 3/50, 22G (0,70) x 50mm, with injection tube and connecting cable · 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 14048223002985), received between Oct 27, 2016 and Oct 27, 2016 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fluid/Blood Leak” (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
- Fluid/Blood Leak1
- Manufacturing, Packaging or Shipping Problem1
- Nonstandard Device1
Patient problems
- Awareness During Anesthesia1
- Inadequate Pain Relief1
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 27, 2016Fluid/Blood Leak; Nonstandard Device; Manufacturing, Packaging or Shipping Problem; Fluid/Blood Leak; Nonstandard Device; Manufacturing, Packaging or Shipping Problem
(B)(4). SUMMARIZING TENTATIVE TRANSLATION FROM INITIAL REPORTER'S NARRATIVE: LEAKAGE AT THE HUB.
Patient problems: Awareness During Anesthesia; Inadequate Pain Relief; No Consequences Or Impact To Patient
MAUDE report 6059532 ↗
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- ARROW IPN922631Teleflex Incorporated · NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)1 recall0 reports
- 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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