McKesson 16-S30CRecalls & reported problems
Mckesson Medical-Surgical Inc. · Syringe, LL 30cc · Class 2
Data updated Oct 16, 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 10612479206943), received between Apr 14, 2024 and Apr 14, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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
- Insufficient Device Problem Information2
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 14, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
THE CUSTOMER REPORT THAT AFTER THE SYRINGE DRAWS UP THE LIQUID, THE LIQUID TURNS YELLOW FROM CLEAR LIQUID.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19102878 ↗MalfunctionApr 14, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
THE CUSTOMER REPORT THAT BARREL RUPTURE. THIS DEFECT WAS RECOGNIZED WHEN THE DRUG WAS INJECTED INTO THE SALINE BAG AFTER IT WAS DRAWN INTO THE SYRINGE. THE SAMPLE ON THE FEEDBACK PHOTO HAS A CRACK IN THE 5ML-20ML REGION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19102877 ↗
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- 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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