Monoject 8881907102Recalls & reported problems
Cardinal Health, Inc. · 10 mL Oral Syringe,Clear · Class 1
- 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 10884521014640), received between Oct 29, 2019 and Oct 29, 2019 — classified as 1 malfunction.
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
Device problems
- Break1
- Crack1
Patient problems
- No Patient Involvement1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 29, 2019Break; Crack; Break; Crack
THE CUSTOMER REPORTED THAT UPON OPENING THE OF CARTONS OF THE SYRINGES, THERE WERE BROKEN PIECES OF SYRINGES INSIDE THE PACKAGING. ADDITIONAL INFORMATION RECEIVED FROM THE CUSTOMER STATED THAT THE TIP OF THE SYRINGES WAS BROKEN AND SOME OF THEM WERE SNAPPED OFF CLEARLY. ALSO, FEW OF THE SYRINGES HAD CRACKED BARRELS. NO PATIENT INVOLVED.
Patient problems: No Patient Involvement
MAUDE report 9252965 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.