McKesson 3077V2Recalls & reported problems
Mckesson Medical-Surgical Inc. · McKesson Epidural Detachable Wing Needle, 20GX3.5 · Class 2
- 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 10612479201719), received between Oct 20, 2017 and Oct 20, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Component Falling” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Component Falling1
Patient problems
- 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 20, 2017Component Falling
THE CUSTOMER REPORTED, THE NEEDLE FELL APART DURING A PROCEDURE. INJECTION WAS COMPLETE AND AS THE NEEDLE WAS BEING REMOVED, THE CLEAR TOP (HUB) CAME OFF AND LEFT THE NEEDLE IN THE PATIENT (WAS INSERTED APPROXIMATELY AN INCH). THE NEEDLE WAS ABLE TO BE REMOVED. NO INJURY OCCURRED TO PATIENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6966778 ↗
Other Needle, Conduction, Anesthetic (W/Wo Introducer) devices
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- ARROW IPN922603Teleflex 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
- 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
- BD QUINCKE Spinal Needles 405180Becton, Dickinson And Company · NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)23 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.