Magellan 8881850110Recalls & reported problems
Cardinal Health, Inc. · Hypodermic Safety Needle · Class 2
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10884521000513), received between Sep 15, 2017 and Oct 10, 2022 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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
- Device Contamination with Chemical or Other Material3
- Fail-Safe Did Not Operate1
- Shielding Failure1
- Use of Device Problem1
Patient problems
- No Consequences Or Impact To Patient4
- Needle Stick/Puncture2
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 10, 2022Fail-Safe Did Not Operate; Fail-Safe Did Not Operate
THE CUSTOMER REPORTED THAT A PARAMEDIC SUFFERED A NEEDLE STICK FROM A DIRTY NEEDLE. THE SAFETY CAP FAILED ON THE DEVICE. PER ADDITIONAL INFORMATION RECEIVED, THE EMPLOYEE HAS RESUMED WORKING AND IS BEING FOLLOWED BY OCCUPATIONAL HEALTH FOR BLOODBORNE EXPOSURE.
Patient problems: Needle Stick/Puncture
MAUDE report 15573553 ↗MalfunctionNov 7, 2019Use of Device Problem; Use of Device Problem
THE CUSTOMER REPORTED THAT THE DEVICE IS PULLING IN AIR/BUBBLES WHEN DRAWING BLOOD. ADDITIONAL INFORMATION RECEIVED STATED THIS HAS HAPPENED SPORADICALLY OVER THE PAST MONTHS.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9290150 ↗MalfunctionDec 26, 2017Shielding Failure; Shielding Failure
THE CUSTOMER REPORTS THAT A NURSE SUSTAINED A NEEDLE STICK WITH PRODUCT WHICH FAILED TO LOCK AFTER SAFETY NEEDLE COVER WAS ADVANCED OVER THE NEEDLE.
Patient problems: Needle Stick/Puncture
MAUDE report 7145586 ↗MalfunctionSep 15, 2017Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
THE CUSTOMER REPORTS THAT AIR IS BEING DRAWN INTO THE SYRINGE WHILST OBTAINING SAMPLES.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6870199 ↗MalfunctionSep 15, 2017Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
THE CUSTOMER REPORTS THAT AIR IS BEING DRAWN INTO THE SYRINGE WHILST OBTAINING SAMPLES. THIS AFFECTS THE QUALITY OF THE SAMPLE RESULTING IN THE PATIENT HAVING TO HAVE ANOTHER VENEPUNCTURE TO OBTAIN A SECOND BLOOD SAMPLE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6869719 ↗MalfunctionSep 15, 2017Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
THE CUSTOMER REPORTS THAT AIR IS BEING DRAWN INTO THE SYRINGE WHILST OBTAINING SAMPLES. THIS AFFECTS THE QUALITY OF THE SAMPLE RESULTING IN THE PATIENT HAVING TO HAVE ANOTHER VENEPUNCTURE TO OBTAIN A SECOND BLOOD SAMPLE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6869405 ↗
Other Needle, hypodermic, single lumen devices
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- BD SafetyGlide 305916Becton, Dickinson And Company · Needle, hypodermic, single lumen1,767 reports
- BD Nano Ultra-Fine 320122Becton Dickinson Pen Limited · Needle, hypodermic, single lumen601 reports
- N/A 305106Becton, Dickinson And Company · Needle, hypodermic, single lumen1 recall467 reports
- N/A 305110Becton, Dickinson And Company · Needle, hypodermic, single lumen418 reports
- BD Safe-Clip 328235Becton, Dickinson and Company Inc · Needle, hypodermic, single lumen268 reports
- BD Ultra-Fine 320109Becton Dickinson Pen Limited · Needle, hypodermic, single lumen229 reports
- BD AutoShield Duo 329515Becton, Dickinson And Company · Needle, hypodermic, single lumen208 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.