Henry Schein 9004473Recalls & reported problems
Henry Schein, Inc. · NDL 23G*1 · Class 2
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00304040002858), received between Sep 11, 2025 and Sep 11, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Dull, Blunt” (2 reports).
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
- Dull, Blunt2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 11, 2025Dull, Blunt; Dull, Blunt
THE CUSTOMER REPORTS THAT THESE ARE NOT SHARP ENOUGH.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23023522 ↗MalfunctionSep 11, 2025Dull, Blunt; Dull, Blunt
OFFICE STATED SOME NEEDLES IN PACK ARE REALLY DULL UNABLE TO PUNCTURE SKIN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23023486 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.