Medline SYR110020Recalls & reported problems
Medline Industries, Inc. · SYRINGE, LUER SLIP, STERILE, 10ML · 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 10888277653559), received between Mar 31, 2024 and Apr 2, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Infusion or Flow Problem” (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
- Infusion or Flow Problem1
- Mechanical Problem1
- Pressure 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.
MalfunctionApr 2, 2024Mechanical Problem; Mechanical Problem
IT WAS REPORTED THAT THE SYRINGE PLUNGER WOULD NOT RETRACT AND "WON'T PULL THE MEDS."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19016922 ↗MalfunctionMar 31, 2024Infusion or Flow Problem; Pressure Problem; Infusion or Flow Problem; Pressure Problem
IT WAS REPORTED THAT THE SYRINGE HAS "TOO MUCH PRESSURE" AND THAT CONTENT "COMES OUT TOO FAST."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19009232 ↗
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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
- 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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