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BD Veo 324906Recalls & reported problems

Becton, Dickinson and Company Inc · BD Veo Insulin Syringes with BD Ultra-Fine Needle, U-100, 6mm, 31G, 0.3mL · 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 30382903249061), received between Dec 7, 2022 and Dec 7, 2022 — classified as 1 malfunction.

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

  • Melted1

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.

  • MalfunctionDec 7, 2022Melted; Melted

    IT WAS REPORTED THAT 5 BD VEO¿ INSULIN SYRINGES WITH BD ULTRA-FINE¿ NEEDLES EXPERIENCED PRODUCT DAMAGE WHILE STILL CONSIDERED OPERABLE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CONSUMER REPORTED FOUND THE TOP OF SYRINGE TO 5 UNITS WERE MELTED. CALLER DREW INTO SYRINGE HUMALOG AND THEN NOTICED THE OUTSIDE OF BARREL TO BE MELTED. CALLER DID NOT INJECT WITH THIS SYRINGE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15936667 ↗

Other Syringe, piston devices

All Syringe, piston devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.