EXEL Hypodermic Disposable Needles 26417Recalls & reported problems
Exel International · EXEL Hypodermic Needle, 20Gx1" · 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 10020221264170), received between Feb 6, 2026 and Feb 6, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Contamination” (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
- Contamination1
- Device Contamination with Chemical or Other Material1
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.
MalfunctionFeb 6, 2026Contamination; Device Contamination with Chemical or Other Material
CALLER REPORTED NEEDLE CONTAMINATION. BLACK PARTICLES WERE FOUND ON THE NEEDLE HUB ON A BRAND-NEW NEEDLE., PRODUCT # 26407, LOT # 240401. NO ADVERSE EVENT REPORTED AS THE CONTAMINATION WAS NOTED RIGHT AWAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24282856 ↗
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- BD Ultra-Fine 320109Becton Dickinson Pen Limited · Needle, hypodermic, single lumen229 reports
- BD AutoShield Duo 329515Becton, Dickinson And Company · Needle, hypodermic, single lumen208 reports
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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