NIPRO SYRINGE JD+03L2219Recalls & reported problems
Nipro Medical Corporation · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00383790000758), received between Dec 21, 2021 and Dec 21, 2021 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Break” (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 18, 2026.
Most reported problems
Device problems
- Break2
Patient problems
- Foreign Body In Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryDec 21, 2021Break; Break
FACILITY REPORTED TWO NEEDLES BREAKING WHEN GIVING IM(INTRAMUSCULAR) INJECTIONS. NO ADDITIONAL INFORMATION HAS BEEN PROVIDED, DATE OF EVENT IS UNKNOWN.
Patient problems: Foreign Body In Patient
MAUDE report 13051775 ↗MalfunctionDec 21, 2021Break; Break
FACILITY REPORTED TWO NEEDLES BREAKING WHEN GIVING IM(INTRAMUSCULAR) INJECTIONS. NO ADDITIONAL INFORMATION HAS BEEN PROVIDED, DATE OF EVENT IS UNKNOWN.
Patient problems: Foreign Body In Patient
MAUDE report 13051729 ↗
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- 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
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- 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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