Henry Schein 1126149Recalls & reported problems
Henry Schein, Inc. · NDL 30G*1 · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 00304040003091), received between Mar 18, 2026 and Mar 18, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Complete Blockage” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Complete Blockage1
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.
MalfunctionMar 18, 2026Complete Blockage
THE CUSTOMER REPORTS THAT WHILE USING EITHER THE 30GA NEEDLE(HS (B)(6)) THEY WERE CLOGGING WHEN MIXING DIFFERENT TYPES OF DRUGS. THESE INCLUDED DEXAMETHASONE, METHYLPREDNISOLONE, MARCAINE AND LIDOCAINE. THIS WAS FOR JOINT INJECTIONS, PLANTAR FASCIA. THE AMOUNTS WOULD BE EITHER OF THE FOLLOWING: A. 2CC LIDOCAINE, .5CC DEXAMETHASONE, .5CC METHYLPREDNISOLONE, B. 2CC MARCAINE, .5CC DEXAMETHASONE, .5CC METHYLPREDNISOLONE, C. 1CC MARCAINE, .25CC DEXAMETHASONE, .25CC METHYLPREDNISOLONE. THIS HAPPENED WITH MULTIPLE PATIENTS OVER THE LAST MONTH, NO SPECIFICS WOULD BE PROVIDED. NO PATIENTS WERE HARMED OR REQUIRED ANY MEDICAL ATTENTION. THERE WAS A DELAY AS THEY HAD TO USE THREE DIFFERENT NEEDLES ON THEIR PATIENTS, WITH MULTIPLE PATIENT OCCURRING WITH MULTIPLE DOCTORS IN THEIR PRACTICE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24625509 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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