Stimuplex® Ultra 360® 333642Recalls & reported problems
B. Braun Medical Inc. · Stimuplex® Ultra 360® 22 Ga. x 2 in. (50 mm) Insulated Echogenic Needle with 30° Bevel and Extension Set (STIMU32250) · 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 04046964726552), 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 20462978 ↗
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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
- 22G 1 1/2IN Regional Block Needle 408348Becton, Dickinson And Company · 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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