Henry Schein 5702705Recalls & reported problems
Henry Schein, Inc. · Needle Disposable Safety 25Gx5/8 · Class 2
Data updated Oct 18, 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 10304040154196), received between Feb 20, 2026 and Feb 20, 2026 — 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 18, 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.
MalfunctionFeb 20, 2026Defective Component
CUSTOMER REPORTS THAT THEY HAD A RECENT NEEDLESTICK INJURY. THEY ARE UNABLE TO DETERMINE WHICH OF THESE LOTS CAUSED THE NEEDLESTICK INJURY AS THESE LOTS WERE IN THE BIN THE NEEDLE WAS STOCKED IN AND THE PACKAGING WAS NOT SAVED WHEN IT WAS BEING USED.
Patient problems: Needle Stick/Puncture
MAUDE report 24398997 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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