Magellan 8881850015Recalls & reported problems
Cardinal Health, Inc. · Hypodermic Safety Needle · Class 2
All models of Magellan (29)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10884521000490), received between Aug 22, 2017 and May 21, 2021 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Device Contaminated During Manufacture or Shipping” (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
- Device Contaminated During Manufacture or Shipping2
- Crack1
- Fluid/Blood Leak1
Patient problems
- No Consequences Or Impact To Patient2
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 21, 2021Crack; Fluid/Blood Leak; Crack; Fluid/Blood Leak
THE CUSTOMER REPORTED THAT WHILE TAPPING BUBBLES OUT OF A MEDICATION THAT WAS DRAWN UP, IT WAS NOTICED THAT THE BOTTOM OF THE NEEDLE WAS CRACKED. THE MEDICATION SPRAYED ONTO THE MA'S ARM. THERE WAS NO HARM TO THE MA OR THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11866650 ↗MalfunctionMay 22, 2018Device Contaminated During Manufacture or Shipping; Device Contaminated During Manufacture or Shipping
THE CUSTOMER REPORTS THAT THERE ARE SMALL IMPURITIES ON THE NEEDLE DUE TO PLASTIC PARTICLES.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7534218 ↗MalfunctionAug 22, 2017Device Contaminated During Manufacture or Shipping; Device Contaminated During Manufacture or Shipping
THE CUSTOMER STATES SOMETHING LIKE HAIR OR PLASTIC IS IN THE NEEDLE WHILE DOING PROCESS FOR MEDICATION. A PATIENT WAS INVOLVED BUT WAS NOT INJURED AND DID NOT REQUIRE MEDICAL INTERVENTION.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6811825 ↗
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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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