inforMED
MalfunctionJQX

BD PHOENIX¿ AP

Received May 22, 2026 · Event occurred Apr 24, 2026

Report 1119779-2026-00840 · MDR key 25257648

Device

Generic name

Nephelometer, For Clinical Use

Catalog number

448010

Product problems

  • Incorrect, Inadequate or Imprecise Result or Readings

Patient

NA · Unknown

  • No Clinical Signs, Symptoms or Conditions

Narrative

Additional Manufacturer Narrative

H3. A DEVICE EVALUATION IS ANTICIPATED BUT HAS NOT YET BEGUN. UPON COMPLETION OF THE INVESTIGATION, A SUPPLEMENTAL REPORT WILL BE FILED.

Description of Event or Problem

IT WAS REPORTED WHILE USING THE BD PHOENIX¿ AP CONTAMINATION OF THE DEVICE OCCURRED. THE USER NOTED THAT THERE WAS AN INCREASE IN VANCOMYCIN-RESISTANT STAPHYLOCOCCUS AUREUS (VRSA). NO HEALTH IMPACT OR CONSEQUENCE REPORTED.