Magellan 8881833215 (UDI 10192253024722)Recalls & reported problems
Cardinal Health 200, LLC · 3 mL Syringe with Hypodermic Safety Needle 22G x 1.5 in. (0.7 x 38 mm) · Class 2
- 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 10192253024722), received between Mar 2, 2022 and Sep 15, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (3 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Fluid/Blood Leak3
- Fail-Safe Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 15, 2026Fail-Safe Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50778231 ↗MalfunctionNov 9, 2022Fluid/Blood Leak; Fluid/Blood Leak
THE CUSTOMER REPORTED THE MEDICATION IS COMING OUT THE SIDE OF THE HUB INSTEAD OF THE NEEDLE ITSELF. IT APPEARS THE HUB IS STRIPPED AND NOT ENGAGING PROPERLY TO THE LUER LOCK.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15758803 ↗MalfunctionJul 21, 2022Fluid/Blood Leak; Fluid/Blood Leak
THE CUSTOMER REPORTED THAT THE SYRINGE CRACKED UNDER PRESSURE. THE SYRINGE DID NOT CRACK UNTIL THE MEDICATION WAS BEING PUSHED INTO THE MUSCLE. IT CRACKED ONCE PRESSURE WAS APPLIED, AND THIS LED TO A PORTION OF THE MEDICATION LEAKING OUT OF THE CRACK. THERE WAS NO HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15078951 ↗MalfunctionMar 2, 2022Fluid/Blood Leak; Fluid/Blood Leak
THE CUSTOMER REPORTED THAT THEY WERE GIVING THE PATIENT WINRHO IM AND AS THE WRITER PUSHED THE PLUNGER ON THE SYRINGE, MEDICATION SHOT OUT WHERE THE SYRINGE MET THE NEEDLE. THE SYRINGE WAS CHECKED PRIOR TO GIVING THE DOSE AND WAS CONNECTED CORRECTLY. THEY WERE UNSURE HOW MUCH MEDICATION THE PATIENT RECEIVED, SO THEY HAD TO GIVE A SECOND DOSE. THE LEAK OCCURRED AT THE GRAY AREA. NO INJURIES OCCURRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13653765 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.