BD QUINCKE Spinal Needles 405234Recalls & reported problems
Becton, Dickinson And Company · NEEDLE SP S/SU 25GA 4-11/16IN QUINCKE · Class 2
All models of BD QUINCKE Spinal Needles (9)
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 00382904052348), received between Oct 2, 2020 and Oct 2, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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
- Device Contamination with Chemical or Other Material1
Patient problems
- No Patient Involvement1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 2, 2020Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
IT WAS REPORTED THAT 2 NEEDLES SP S/SU 25GA 4-11/16IN QUINCKE FROM LOT 8285784, AND 1 NEEDLE FROM LOT 9035553 HAD DARK FLECKS OF FOREIGN RESIDUE ON THEM BEFORE USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "HARD RESIDUE FLECKS HAVE BEEN FOUND ON A FEW BD REF# (B)(4) QUINCKE NEEDLES. APPROXIMATELY 3-4 OF THESE NEEDLES HAD A SMALL, DARK COLORED FLECK OF RESIDUE ATTACHED TO THE SHAFT OF THE NEEDLE. THIS HAS BEEN OVER THE PAST SIX MONTHS AND ONLY ONE NEEDLE WILL SHOW A DEFECT AT ANY TIME GIVEN. THESE NEEDLES COME FROM AT LEAST TWO DIFFERENT LOT NUMBERS, INCLUDING LOT# 8285784 AND LOT #9035553. NONE OF THE DEFECTIVE NEEDLES WERE USED FOR PROCEDURE."
Patient problems: No Patient Involvement
MAUDE report 10624089 ↗
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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 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
- BD QUINCKE Spinal Needles 405180Becton, Dickinson And Company · NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)23 reports
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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