EXEL Syringes 26115Recalls & reported problems
Exel International · EXEL Disposable Syringe with Needle, 3mL Luer Lock Tip W/ 22Gx3/4" · Class 2
Data updated Oct 18, 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 00020221261158), received between Nov 22, 2017 and Oct 29, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Detachment Of Device 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
- Detachment Of Device Component1
- No Apparent Adverse Event1
Patient problems
- Needle Stick/Puncture1
- No Code Available1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 29, 2025No Apparent Adverse Event; No Apparent Adverse Event
CALLER REPORTED THEY COULD NOT DRAW AIR IN OR OUT OF THE SYRINGE. WHILE TRYING TO DO SO CUSTOMER ACCIDENTALLY STABBED THEIR FINGER WITH THE NEED AND INJECTED AIR INTO THEMSELVES. CUSTOMER WENT TO THE ER AND DOCTOR DID NOT HAVE TO TAKE ANY ACTION UPON OBSERVATION. NO SUBSTANTIAL DAMAGE OCCURRED TO THE PATIENT.
Patient problems: Needle Stick/Puncture
MAUDE report 23418518 ↗MalfunctionNov 22, 2017Detachment Of Device Component; Detachment Of Device Component
THE DOG (CANINE, (B)(6))) WAS INJECTED SUBCUTANEOUSLY WHILE RESTRAINED BY A VETERINARY TECHNICIAN. DURING THE INJECTION, THE NEEDLE BROKE OFF THE HUB AND BECAME LODGED UNDER THE SKIN. THE ATTENDING DVM PLACED THE DOG UNDER GENERAL ANESTHESIA AND SURGICALLY REMOVED THE NEEDLE.
Patient problems: No Code Available
MAUDE report 7054363 ↗
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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