Henry Schein 1127103Recalls & reported problems
Henry Schein, Inc. · NDL 27G*1 1/4 · Class 2
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00304040002940), received between Sep 11, 2025 and Mar 31, 2026 — classified as 3 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
- Complete Blockage1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 31, 2026Dull, Blunt
THE PATIENTS ARE REPORTING THE NEEDLE POKES SEEM MORE PAINFUL THAN USUAL, ALMOST LIKE THE NEEDLES ARE MORE DULL THAN NORMAL. ADDITIONAL QUESTIONS WERE EMAILED TO (B)(6) (HS FIELD REP), AND HE FORWARDED THE QUESTIONS TO THE CUSTOMER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24740502 ↗MalfunctionMar 18, 2026Complete Blockage
THE CUSTOMER REPORTS THAT EVERY SINGLE ONE THEY USE IS GETTING CLOGGED. THEY USE KENALOG, LIDOCAINE AND MARCAINE. IT HAPPENED TO 14 OF THE PATIENTS WITH TWO DIFFERENT DOCTORS. ALL OF THE PROCEDURES ARE ON THE FEET, ANKLE, INTERSPACSM, NUEROMA, HEEL TRIGGER POINTS AND SINUS TARSI INJECTIONS.NO PATIENTS WERE HARMED OR REQUIRED ANY MEDICAL ATTENTION. IT HAPPENED ON (B)(6) 2026. NO PATIENT SPECIFICS PROVIDED. NO PHOTOS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24631250 ↗MalfunctionSep 11, 2025Dull, Blunt; Dull, Blunt
THE CUSTOMER ADVISED THAT THE NEEDLES ARE DULL AND CANNOT BE USED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23023543 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.