Henry Schein 5702693Recalls & reported problems
Henry Schein, Inc. · Needle Disposable Safety 18Gx1 · 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 10304040154059), received between Aug 22, 2025 and Aug 22, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Defective 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. 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
- Defective Component1
Patient problems
- Needle Stick/Puncture1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 22, 2025Defective Component; Defective Component
THE CUSTOMER REPORTS THAT A 39-YEAR-OLD MALE PARAMEDIC WAS DRAWING UP MEDICATION AND WAS WEARING GLOVES. THE SAFETY CLASP WAS NOT ENGAGING. THIS THEN RESULTED IN A NEEDLESTICK INJURY FROM A USED NEEDLE. IT WAS NOT DOCUMENTED IF THE PERSON WEARING HAD ANY OPEN CUTS. THE PARAMEDIC CLEANED THE AREA WITH SOAP AND WATER AND APPLIED BANDAGE TO THE AREA.
Patient problems: Needle Stick/Puncture
MAUDE report 22870264 ↗
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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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