Medline SYRS103235Recalls & reported problems
Medline Industries, Inc. · SAFETY SYRINGE, 3ML 23GX1" · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 30888277222575), received between Apr 5, 2024 and Apr 6, 2024 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (3 reports).
1 FDA recall record name this device's identifier, 1 still open.
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
Recalls naming this device
- May 9, 2024Open, Classified
Products in distribution were found by FDA to be to be substantially different from the current cleared 510(k)s with a major change or modification to the device s intended use.
Z-3074-2024 · Root cause: Other · Recall details · FDA record ↗
Most reported problems
Device problems
- Detachment of Device or Device Component3
- Failure to Align1
- Loose or Intermittent Connection1
- Material Twisted/Bent1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 6, 2024Detachment of Device or Device Component; Material Twisted/Bent; Detachment of Device or Device Component; Material Twisted/Bent
IT WAS REPORTED THAT THE SYRINGE WAS RECEIVED WITH THE NEEDLE UNATTACHED AND THAT THE NEEDLE WAS BENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19056737 ↗MalfunctionApr 6, 2024Failure to Align; Detachment of Device or Device Component; Failure to Align; Detachment of Device or Device Component
IT WAS REPORTED THAT THE NEEDLE DETACHED FROM THE SYRINGE WHEN ATTEMPTING TO ACTIVITY THE NEEDLE SAFETY FEATURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19056733 ↗MalfunctionApr 6, 2024Loose or Intermittent Connection; Loose or Intermittent Connection
IT WAS REPORTED THAT, TWICE, THE NEEDLE BECAME LOOSE FROM THE SYRINGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19056518 ↗MalfunctionApr 5, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT THE NEEDLE WAS "FLIMSY" AND THAT IT BROKE OFF THE SYRINGE DURING USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19052120 ↗
Other Syringe, piston devices
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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
- 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 · each recall links to the FDA recall notice
- 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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