BD Perisafe™ 405074Recalls & reported problems
Becton, Dickinson And Company · NEEDLE SPINAL S/SU 22GA 2-1/2IN QUINCKE · Class 2
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00382904050740), received between Nov 27, 2018 and Nov 21, 2024 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Leak/Splash” (2 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
- Leak/Splash2
- Contamination of Device Ingredient or Reagent1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 21, 2024Leak/Splash; Leak/Splash
MATERIAL # 405074 BATCH # 4166281. WE HAVE HAD SEVERAL REPORTED EVENTS OF LEAKING WHEN USING THIS SYRINGE WITH A LUER SPINAL NEEDLE (ITEM 405074 22G X 2.5IN QUINCKE NEEDLE) TO ADMINISTER INTRATHECAL CHEMOTHERAPY. THIS IS CAUSING CONCERN DUE TO HAZARDOUS DRUG EXPOSURE AND THE RISK THAT A PATIENT WON¿T RECEIVE THE FULL AMOUNT OF CHEMOTHERAPY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20747334 ↗MalfunctionNov 21, 2024Leak/Splash; Leak/Splash
MATERIAL #: 405074; BATCH#: 4166281. IT WAS REPORTED BY CUSTOMER THAT THEY HAD SEVERAL REPORTED EVENTS OF LEAKING WHEN USING THIS SYRINGE WITH A LUER SPINAL NEEDLE (ITEM 405074 22G X 2.5IN QUINCKE NEEDLE) TO ADMINISTER INTRATHECAL CHEMOTHERAPY. THIS IS CAUSING CONCERN DUE TO HAZARDOUS DRUG EXPOSURE AND THE RISK THAT A PATIENT WON¿T RECEIVE THE FULL AMOUNT OF CHEMOTHERAPY.
Patient problems: Insufficient Information
MAUDE report 20745011 ↗MalfunctionNov 27, 2018Contamination of Device Ingredient or Reagent
IT WAS REPORTED WITH THE USE OF THE BD¿ QUINCKE SPINAL NEEDLE THERE WAS AN ISSUE WITH FOREIGN MATTER. THERE WAS NO REPORT OF INJURY OR MEDICAL INTERVENTION.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8106304 ↗
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- 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.