Magellan 8881893010Recalls & reported problems
Cardinal Health, Inc. · 1 mL Insulin Safety Syringe,Permanent 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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10884521005952), received between Aug 18, 2020 and Mar 14, 2024 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Fail-Safe Problem” (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.
Reports received per month
Most reported problems
Device problems
- Fail-Safe Problem1
Patient problems
- Needle Stick/Puncture2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 14, 2024
REGISTERED NURSE (RN) WAS DRAWING UP LANTUS AND WENT TO RECAP THE NEEDLE TO TAKE TO THE PATIENT. THE NEEDLE WENT THROUGH THE CAP AND STUCK THE RN. THE RN IS UNAWARE OF ANY MEDICATION WENT INTO HER. RN IMMEDIATELY CLEANED THE AREA AND THREW OUT THE NEEDLE.
Patient problems: Needle Stick/Puncture
MAUDE report 18902189 ↗InjuryAug 18, 2020Fail-Safe Problem; Fail-Safe Problem
THE CUSTOMER REPORTED THAT THE NURSE WAS ADMINISTERING SC INSULIN AND AFTER THE PROCEDURE SHE WENT TO USE THE SAFETY CATCH AND THE NEEDLE PUNCTURED THROUGH THE SIDE OF THE SAFETY CATCH RESULTING IN A NEEDLE STICK INJURY. THE PATIENT IS (B)(6). THE SAFETY SHIELD WAS ACTIVATED BY THE NURSE WITH HER HANDS AND IT MOVED FREELY BUT THE NEEDLE CAME OUT OF THE SIDE. THE CUSTOMER IS UNSURE IF AN AUDIBLE CLICK WAS HEARD AFTER ACTIVATING THE SHIELD. THE NURSE WAS GIVEN A (B)(6) BOOSTER AND BLOODS FOR STORAGE. BLOOD TEST WERE COMPLETED AND ALL RESULTS WERE NORMAL. THE NURSE WILL BE GIVEN A (B)(6)BOOSTER AS FOLLOW UP MEDICAL INTERVENTION.
Patient problems: Needle Stick/Puncture
MAUDE report 10423088 ↗
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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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