Monoject 8881200060Recalls & reported problems
Cardinal Health, Inc. · Standard Hypodermic Needle,Aluminum Hub · 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 30884521007639), received between Dec 20, 2023 and Dec 20, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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
- Detachment of Device or Device Component1
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 20, 2023Detachment of Device or Device Component; Detachment of Device or Device Component
THE CUSTOMER REPORTED THAT WHEN USING THEM THEY WERE BREAKING OFF FROM THE HUB. THAT HAPPENED TO A HANDFUL OUT OF THE BOX AND THEY STOPPED USING IT WHEN THE LAST ONE BROKE AND THEY HAD TO PULL IT OUT OF THE COW THAT WAS IN THE CHUTE. ADDITIONAL INFORMATION RECEIVED ON 13DEC2023 STATED THAT THE NEEDLE DETACHED FROM THE HUB, AND WERE ONLY USED ON CATTLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18369560 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.