Magellan 7777850215Recalls & reported problems
Cardinal Health 200, LLC · Magellan, Hypodermic Safety Needle, Black Hub 22 G x 1-1/2" (0.7 mm x 38 mm) · Class 2
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10884521155527), received between Jun 21, 2017 and Sep 27, 2017 — classified as 4 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
- Crack2
Patient problems
- No Known Impact Or Consequence To Patient3
- No Consequences Or Impact To Patient1
- No Information1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 27, 2017Break; Break
MalfunctionJun 28, 2017Break; Break
THE CUSTOMER REPORTS THE NEEDLE HAS A BROKEN HUB.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6675140 ↗MalfunctionJun 21, 2017Crack; Crack
THE CUSTOMER REPORTS A BROKEN HUB. TO POST MARKET SURVEILLANCE TEAM: - PLEASE PROVIDE A LETTER OF CLOSE OUT/OFFICIAL CONCLUSION OF THE QUALITY COMPLAINT AND SEND TO: (B)(4) IMPORTANT SPECIFIC COMMENTS: FOR MEDTRONIC LOT 609905 MENTIONED IN THIS REPORT. NO MORE INFORMATION WAS PROVIDED TO STERIPACK AND NO MORE INFORMATION WILL BE PROVIDED TO MEDTRONIC. . THANKS DETAILS OF THE EVENT COMMUNICATED BY (B)(4): "WE RECEIVED COMPLAINT FROM OUR CUSTOMER REGARDING BROKEN HUB".-###-FROM (B)(4)-THE CUSTOMER REPORTS A BROKEN HUB.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 6657835 ↗MalfunctionJun 21, 2017Crack; Crack
THE CUSTOMER REPORTED A BROKEN HUB.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6656759 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.