Medline SYRA101272Recalls & reported problems
Medline Industries, Inc. · ALLERGY TRAY, 27GX0.5", 1ML · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10888277654082), received between Apr 6, 2024 and Sep 23, 2026 — classified as 7 malfunctions.
The most frequently reported specific device problem is “Dull, Blunt” (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
- Dull, Blunt2
- Fluid/Blood Leak2
- Insufficient Device Problem Information2
- Leak/Splash1
- Material Too Soft/Flexible1
Patient problems
- No Clinical Signs, Symptoms or Conditions6
- Discomfort1
- Pain1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 23, 2026Dull, Blunt
Patient problems: No Clinical Signs, Symptoms or Conditions; Pain
MAUDE report 50875085 ↗MalfunctionSep 21, 2026Dull, Blunt
It was reported that "the needles are dull" and "The needle are not puncturing effectivly."
Patient problems: Discomfort
MAUDE report 50841147 ↗MalfunctionNov 6, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
CUSTOMER FEEDBACK: SYRINGE LEAKAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20617803 ↗MalfunctionNov 6, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
CUSTOMER FEEDBACK: LEAKING AND THE NEEDLES ARE BENDING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20617621 ↗MalfunctionApr 8, 2024Leak/Splash; Leak/Splash
ACCORDING TO THE CUSTOMER, "AFTER DRAWING UP THE SERUM FROM THE VIALS AND PULLING THE NEEDLE OUT OF THE STOPPER, SOME NEEDLES WOULD DRIBBLE SOLUTION OUT THE END OF THE NEEDLE, CAUSING A DOSE CHANGED".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19060719 ↗MalfunctionApr 6, 2024Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED THAT THE SYRINGE LEAKED WHEN DRAWING BACK THE SYRINGE PLUNGER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19056735 ↗MalfunctionApr 6, 2024Fluid/Blood Leak; Material Too Soft/Flexible; Fluid/Blood Leak; Material Too Soft/Flexible
IT WAS REPORTED THAT THE SYRINGE WAS LEAKING AND THAT THE NEEDLE WAS NOTED TO BE "BENDING."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19056517 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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