McKesson 16-ST1CRecalls & reported problems
Mckesson Medical-Surgical Inc. · Syringe, TB w/o NDL, 1 cc · 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 10612479207353), received between Apr 13, 2024 and Apr 13, 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 13, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
NEEDLE DISLODGEMENT (THE SYRINGE NEEDLE FALLS OUT DURING INJECTION AFTER THE SYRINGE IS LOADED WITH A NEEDLE BARREL).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19102811 ↗MalfunctionApr 13, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
SYRINGE LEAKS (SYRINGES WILL KEEP SPINNING AFTER BEING FILLED WITH A METAL SYRINGE, TIGHTENED AND THEN CONTINUED TO BE TWISTED HARD).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19102810 ↗
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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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