McKesson 26548Recalls & reported problems
Mckesson Medical-Surgical Inc. · SYRINGE/NDL, SAFETY 3CC 25GX1 · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10612479201085), received between Jun 7, 2019 and Aug 20, 2019 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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.
Most reported problems
Device problems
- Detachment of Device or Device Component2
- Mechanical Jam2
Patient problems
- No Consequences Or Impact To Patient4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 20, 2019Mechanical Jam; Mechanical Jam
THE CUSTOMER REPORTED THAT THE PLUNGER FELT STICKY AND THAT THE NURSE COULDN'T PUSH MEDICATION (B12) INTO THE PATIENT'S ARM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8911278 ↗MalfunctionAug 20, 2019Mechanical Jam; Mechanical Jam
THE CUSTOMER REPORTED THAT THE PLUNGER FELT STICKY AND THAT THE NURSE COULDN'T PUSH MEDICATION (B12) INTO THE PATIENT'S ARM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8911272 ↗MalfunctionJun 7, 2019Detachment of Device or Device Component; Detachment of Device or Device Component
CUSTOMER REPORTS: NEEDLE IS EXTREMELY LOOSE AND NOT ATTACHED TO THE SYRINGE. PER ADDITIONAL INFORMATION RECEIVED ON 06/03/19,: THE ENTIRE UNIT BECAME UNSCREWED FROM THE SYRINGE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8678681 ↗MalfunctionJun 7, 2019Detachment of Device or Device Component; Detachment of Device or Device Component
THE CUSTOMER REPORTED THAT DURING THE ADMINISTRATION OF AN INJECTION, THE NEEDLE DETACHED FROM THE SYRINGE BODY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8678678 ↗
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- BD Luer-Lok 309653Becton, Dickinson And Company · Syringe, piston948 reports
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- BD Plastipak Syringe 300865Becton, Dickinson And Company · Syringe, piston515 reports
- 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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