Magellan 7777850310Recalls & reported problems
Cardinal Health, Inc. · Magellan, Safety Needle, 23 G x 1” (0.635 mm x 2.5 cm), Caution: For processing, repacking or manufacturing · Class 2
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10884521155534), received between Jun 15, 2017 and Jun 28, 2019 — classified as 7 malfunctions.
The most frequently reported specific device problem is “Break” (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.
Most reported problems
Device problems
- Break3
- Device Contaminated During Manufacture or Shipping2
- Crack1
- Leak/Splash1
- Loose or Intermittent Connection1
Patient problems
- No Known Impact Or Consequence To Patient5
- No Information2
- No Consequences Or Impact To Patient1
- No Patient Involvement1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 28, 2019Device Contaminated During Manufacture or Shipping; Device Contaminated During Manufacture or Shipping
THE CUSTOMER REPORTED THAT A FOREIGN MATERIAL IMBEDDED IN THE PLASTIC ON THE ONE PIECE OF COMPONENT. ADDITIONAL INFORMATION RECEIVED FROM THE CUSTOMER STATES THE CONTAMINATION IS ON THE SHIELD AND THE HUB. THE CUSTOMER ALSO MENTIONED THAT THEY CANNOT CONFIRM THAT THE PARTICLE WOULDN'T BE ON THE FLUID PATH.
Patient problems: No Patient Involvement
MAUDE report 8743971 ↗MalfunctionAug 1, 2018Loose or Intermittent Connection; Device Contaminated During Manufacture or Shipping; Device Contaminated During Manufacture or Shipping
THE CUSTOMER REPORTS: DURING PRODUCTION PROCESS, THE NEEDLES WITH LOOSE PARTICLES WERE FOUND.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 7739850 ↗MalfunctionAug 16, 2017Break; Break
CUSTOMER REPORTS THE HUB OF THE NEEDLE IS BROKEN.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6798133 ↗MalfunctionAug 15, 2017Leak/Splash; Leak/Splash
THE CUSTOMER REPORTED BROKEN HUB. THERE WAS A LEAK OF PRODUCT BETWEEN THE SYRINGE AND THE NEEDLE AT THE DE-AERATION TIME ¿DELTOID 1¿/BLUE HUB.
Patient problems: No Information; No Known Impact Or Consequence To Patient
MAUDE report 6795791 ↗MalfunctionJun 26, 2017Break; Break
THE CUSTOMER REPORTS THE HUB OF THE NEEDLE IS BROKEN.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6666869 ↗MalfunctionJun 21, 2017Crack; Crack
MalfunctionJun 15, 2017Break; Break
THE CUSTOMER REPORTED BROKEN HUB WITH THE NEEDLES AND LOOSE PARTICLES WERE FOUND.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6644955 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.