McKesson 306619Recalls & reported problems
Mckesson Medical-Surgical Inc. · Syringes with Safety Hypodermic Needles GLIDE|Thin wall/ Luer Lock 3cc 25G x 1 in (50/bx, 8/cs) · Class 2
- 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 10612479262741), received between Sep 5, 2023 and Dec 12, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Complete Blockage” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Complete Blockage1
- Volume Accuracy 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.
MalfunctionDec 12, 2025Volume Accuracy Problem; Volume Accuracy Problem
THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL # 306619 BATCH # 5034227. VERBATIM: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. COMPLAINT NUMBER (B)(4). REPORT DATE 11/18/2025. FACTORY/MANUFACTURER BECTON DICKINSON. MFR REORDER # (B)(4). PRODUCT NAME SYR/NDL, SFTY (B)(6) LOT / SERIAL NUMBER (B)(6). PRODUCT CONCERN GRADUATIONS ARE NOT CORRECT ON SYRINGE. ADDITIONAL INFORMATION PROVIDED: "WHEN DRAWING UP VACCINES WITH EITHER OF THEM THEY USUALLY ONLY CAME BETWEEN 0.3-0.4 ML IN VOLUME INSTEAD OF 0.5 ML".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23796449 ↗MalfunctionSep 5, 2023Complete Blockage; Complete Blockage
(B)(4) ADDITIONAL INFORMATION RECEIVED. MAT#: 306619, BATCH#:2236328. IT WAS REPORTED BY THE CUSTOMER THAT SYRINGE WON'T PUSH FORWARD. VERBATIM: RCC RECEIVED THE COMPLAINT VIA EMAIL. MFR REORDER # 192-(B)(6). PRODUCT NAME SYR/NDL, SFTY 192-(B)(6) ORG3CC 25GX1." LOT / SERIAL NUMBER: (B)(6). PRODUCT CONCERN: SYRINGE WON'T PUSH FORWARD.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17686094 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.