Magellan 7777866210Recalls & reported problems
Cardinal Health, Inc. · Magellan, Safety Needle, Pink Hub, 22 G x 1” (0.711 mm x 2.5 cm) TW, Caution: For processing, repacking or manufacturing · Class 2
Data updated Oct 13, 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 10884521201927), received between Aug 16, 2017 and Aug 21, 2017 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Break2
Patient problems
- No Known Impact Or Consequence To Patient2
- No Patient Involvement1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 21, 2017Break; Break
THE CUSTOMER REPORTS THE HUB OF THE NEEDLE IS BROKEN.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6808256 ↗MalfunctionAug 16, 2017Break; Break
THE CUSTOMER REPORTS THE HUB OF THE NEEDLE IS BROKEN.
Patient problems: No Known Impact Or Consequence To Patient; No Patient Involvement
MAUDE report 6797988 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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