Spinocan® 333320Recalls & reported problems
B. Braun Medical Inc. · Spinocan® 22 Ga. x 3-1/2 in. (90 mm) Spinal Needle · Class 2
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 04046964833236), received between Jun 30, 2026 and Sep 29, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Contamination /Decontamination Problem” (4 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Contamination /Decontamination Problem4
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Contamination /Decontamination Problem
This report has been identified as B. Braun Medical internal number (b)(4).As reported by the user facility:It was reported that the needles have a green substance on the hub. No injury reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50928062 ↗MalfunctionSep 29, 2026Contamination /Decontamination Problem
This report has been identified as B. Braun Medical internal number (b)(4).As reported by the user facility:It was reported that the needles have a green substance on the hub. No injury reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50928058 ↗MalfunctionSep 14, 2026Contamination /Decontamination Problem
As reported by the user facility:The needle used during a procedure had a residue on the top where the stylet is. No injury reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50751306 ↗MalfunctionJun 30, 2026Contamination /Decontamination Problem
AS REPORTED BY THE USER FACILITY: THERE IS A GREEN FILM OR "GOO" WHICH IS CAUSING THE HUB TO STICK TO THE CANNULA WHEN DOING INJECTIONS AND GOING TO WITHDRAWAL THE NEEDLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25665730 ↗
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- ARROW IPN923597Teleflex Incorporated · NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)1 recall0 reports
- ARROW IPN922631Teleflex Incorporated · NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)1 recall0 reports
- ARROW IPN922604Teleflex Incorporated · NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)1 recall0 reports
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.