Magellan 8881850810Recalls & reported problems
Cardinal Health, Inc. · Hypodermic Safety Needle · Class 2
All models of Magellan (29)
Data updated Oct 18, 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 10884521000582), received between Aug 30, 2019 and Sep 15, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Crack” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Crack1
- Fail-Safe Did Not Operate1
- Fail-Safe Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Information1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 15, 2026Fail-Safe Did Not Operate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50779402 ↗MalfunctionFeb 13, 2020Fail-Safe Problem; Fail-Safe Problem
THE CUSTOMER REPORTED THAT THE SAFETY MECHANISM SNAPPED OFF OF THE DEVICE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9707586 ↗MalfunctionAug 30, 2019Crack; Crack
THE CUSTOMER REPORTED THAT THE HUB CRACKED WHERE IT ATTACHES TO THE SYRINGE CAUSING THE MEDICATION/VACCINATION TO LEAK OUT.
Patient problems: No Information
MAUDE report 8949694 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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