Magellan 8881850915Recalls & 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
- 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 10884521000667), received between Apr 17, 2018 and Sep 26, 2018 — classified as 2 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 16, 2026.
Most reported problems
Device problems
- Crack1
- Device Contaminated During Manufacture or Shipping1
Patient problems
- No Patient Involvement2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 26, 2018Device Contaminated During Manufacture or Shipping; Device Contaminated During Manufacture or Shipping
THE CUSTOMER STATES: DURING SAMPLING, THEY OBSERVED A BLACK COLORING INSIDE THE BLISTER OF NEEDLE GUARD AND THE BLISTER IS NOT CORRECTLY PLACED IN TWO DIFFERENT PLACES. THE NEEDLE ITSELF HAS THE BLACK COLORING ON IT AS WELL.
Patient problems: No Patient Involvement
MAUDE report 7910081 ↗MalfunctionApr 17, 2018Crack; Crack
THE CUSTOMER STATES THE HUB OF THE NEEDLE IS CRACKED.
Patient problems: No Patient Involvement
MAUDE report 7436120 ↗
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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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