Stimuplex® Ultra 360® 333648Recalls & reported problems
B. Braun Medical Inc. · Stimuplex® Ultra 360® 20 Ga. x 4 in. (100 mm) Insulated Echogenic Needle with 30° Bevel and Extension Set (STIMU320100) · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04046964726613), received between Oct 16, 2024 and Oct 16, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Sharp Edges” (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
- Sharp Edges1
Patient problems
- Nerve Damage1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 16, 2024Sharp Edges; Sharp Edges
AS REPORTED. BRIEF INQUIRY DESCRIPTION. NERVE DAMAGE FROM NEEDLE SHARPNESS. DETAILED INQUIRY DESCRIPTION. THE BRAUN ONES (NEEDLES) WILL PIERCE THE NERVE SINCE IT'S SHARPER. ANESTHESIA IS HAVING ISSUES AT COPPER RIDGE WITH NERVE INJURIES. 2 SEPARATE EXPERIENCED PROVIDERS AROUND THE SAME TIME HAD PERMANENT POPLITEAL NERVE INJURIES AT OUR SURGERY CENTER USING THE BRAUN NEEDLES.
Patient problems: Nerve Damage
MAUDE report 20463178 ↗
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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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