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Devon 31142386Recalls & reported problems

Cardinal Health, Inc. · 1920 Foam Block Needle Counter · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30884527016420), received between Dec 5, 2019 and Dec 5, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Material Puncture/Hole” (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

  • Material Puncture/Hole1

Patient problems

  • Needle Stick/Puncture1

Recent adverse event reports

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

  • InjuryDec 5, 2019Material Puncture/Hole; Material Puncture/Hole

    CUSTOMER REPORTS THAT NEEDLE HAS SPLICED THROUGH THE NEEDLE COUNTER. THE INCIDENT HAS LED TO A CONTAMINATED SHARPS INJURY.

    Patient problems: Needle Stick/Puncture

    MAUDE report 9416764 ↗

Other NEEDLE, SUTURING, DISPOSABLE devices

All NEEDLE, SUTURING, DISPOSABLE devices →

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