BD Perisafe™ 405078Recalls & reported problems
Becton, Dickinson And Company · NEEDLE SPINAL S/SU 25GA 2IN QUINCKE · 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 00382904050788), received between Feb 18, 2025 and Feb 18, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Complete Blockage” (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.
Reports received per month
Most reported problems
Device problems
- Complete Blockage1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 18, 2025Complete Blockage; Complete Blockage
MATERIAL # 405078 BATCH # 4094878 VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. 25 X 2 SPINAL NEEDLE WAS BEING USED FOR A PATIENT'S INJECTION, AND WHEN TRYING TO INJECT MEDICATION THERE WAS RESISTANCE AND IT WAS OCCLUDED. NEEDLE WAS REMOVED AND STYLET WAS PLACED BACK IN TO SEE IF THERE WAS STILL AN OCCLUSION. THE STYLET HELPED WITH THE OCCLUSION AND THEN INJECTION WAS ABLE TO BE FINISHED. THIS IS THE SECOND NEEDLE FROM THIS LOT 4094878 TO HAVE AN OCCLUSION AT THE BEGINNING OF PROCEDURE. DATE OF EVENT: (B)(6)2025 NO HARM TO PATIENT
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21407185 ↗
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- ARROW IPN923597Teleflex 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.