EXEL Syringes 26102Recalls & reported problems
Exel International · EXEL Disposable Syringe with Needle, 3mL Luer Lock Tip W/ 22Gx1" · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00020221261028), received between Sep 5, 2025 and Oct 31, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Disconnection” (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. 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
- Disconnection2
- Connection Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 31, 2025Disconnection; Connection Problem; Disconnection; Connection Problem
CUSTOMER REPORTED EXPERIENCING ISSUE AND MENTIONED THAT EXEL 26102 3 ML SYRINGE 2/22G X 1" NEEDLES ARE NOT ATTACHED PROPERLY AND THEY ARE LEAKING. THERE WERE NO ADVERSE EVENT REPORTED TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23442759 ↗MalfunctionSep 5, 2025Disconnection; Disconnection
1 FULL BOX SYRINGE EXEL 3CC LL 22X1 100S HAVE AN ISSUE WITH THE LL BEING LOOSE AND NOT TIGHTENING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22986626 ↗
Other Syringe, Piston devices
- BD Luer-Lok 309657Becton, Dickinson And Company · Syringe, piston1,266 reports
- BD Luer-Lok 309653Becton, Dickinson And Company · Syringe, piston948 reports
- BD Luer-Lok 309628Becton, Dickinson And Company · Syringe, piston862 reports
- N/A 302995Becton, Dickinson And Company · Syringe, piston1 recall537 reports
- BD Plastipak Syringe 300865Becton, Dickinson And Company · Syringe, piston515 reports
- N/A 302830Becton, Dickinson And Company · Syringe, piston462 reports
- N/A 302832Becton, Dickinson And Company · Syringe, piston424 reports
- BD Ultra-Fine 328468Becton, Dickinson and Company Inc · Syringe, piston323 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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