BD Perisafe™ 405140Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00382904051402), received between Feb 20, 2024 and Feb 20, 2024 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (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

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 20, 2024Break; Break

  MATERIAL#: 405140 LOT#: UNKNOWN IT WAS REPORTED BY CUSTOMER THAT AHS RECEIVED A MEDICAL DEVICE INCIDENT REPORT THAT INVOLVED BD SPINAL NEEDLE (CODE: 405140) WITH ADVERSE PATIENT IMPACT/POTENTIAL ADVERSE PATIENT IMPACT. VERBATIM: AHS RECEIVED A MEDICAL DEVICE INCIDENT REPORT THAT INVOLVED BD SPINAL NEEDLE (CODE: 405140 )WITH ADVERSE PATIENT IMPACT/POTENTIAL ADVERSE PATIENT IMPACT. HI BD TEAM AHS RECEIVED A MEDICAL DEVICE INCIDENT REPORT THAT INVOLVED BD SPINAL NEEDLE (CODE: 405140 )WITH ADVERSE PATIENT IMPACT/POTENTIAL ADVERSE PATIENT IMPACT. AHS MDIP NUMBER: 38100 DATE OF MDIP (YYYY-MM-DD): (B)(6) 2024 ADVERSE EFFECT: HARM OR POTENTIAL FOR CLINICALLY SERIOUS ADVERSE EVENT DEVICE AVAILABLE FOR INVESTIGATION: YES REPORTED DEVICE: WHITEACRE PENCIL POINT SPINAL NEEDLE REPORTED DEVICE MANUFACTURER CODE: 405140 15FEB2024: PER CUSTOMER RESPONSE: DATE OF INCIDENT (YYYY-MM-DD): (B)(6) 2024 WHAT WAS THE TYPE OF INCIDENT/PROBLEM? A2. FAILURE (I.E. WHILE PREPARING FOR, IN USE, AFTER USE) WHAT WAS THE LEVEL OF HARM?: HARM OR CLINICALLY SERIOUS ADVERSE EVENT AHS REPORT TO HEALTH CANADA: YES WHAT ARE THE DETAILS OF THE INCIDENT?: END OF SPINAL NEEDLE BROKE OFF WHEN REMOVING INTRODUCER FROM PATIEN

  Patient problems: Device Embedded In Tissue or Plaque

  MAUDE report 18739029 ↗