Magellan 8881833110Recalls & reported problems
Cardinal Health 200, LLC · 3 mL Syringe with Hypodermic Safety Needle 21G x 1" (0.8 x 25 mm) · Class 2
All models of Magellan (9)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10192253024692), received between Aug 18, 2023 and Aug 18, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Use of Device 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.
Most reported problems
Device problems
- Use of Device Problem1
Patient problems
- Eye Injury1
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 18, 2023Use of Device Problem; Use of Device Problem
THE CUSTOMER REPORTED THAT THERE WAS A CATARACT EXTRACTION WAS PERFORMED ON (B)(6) 2023, FOLLOWED BY IMPLANT OF THE LENS AS SCHEDULED. AFTER THE IMPLANT OF THE LENS, THE SURGEON WAS GIVEN A 3ML SYRINGE FILLED WITH 3ML OF BSS (BALANCED SALT SOLUTION) WITH A HYDRODISSECTION NEEDLE ATTACHED. THE SURGEON INSERTED THE NEEDLE TO THE INCISION AND IT WAS THEN NOTED THAT THE FLUID CAME OUT OF THE EYE QUICKLY AND THE SYRINGE WAS VISUALIZED BY AN ASSOCIATE TO BE IN THE SURGEON'S HAND WITHOUT THE NEEDLE ATTACHED TO THE SYRINGE, BUT WAS STILL LOCATED IN THE INCISION. THE SURGEON THEN VIEWED THE NEEDLE THROUGH THE MICROSCOPE AND REMOVED IT. THE SURGEON INFORMED THE SURGICAL TEAM THAT THE LENS WOULD NEED TO BE REMOVED AND A VITRECTOMY WOULD NEED TO BE PERFORMED. THE PATIENT SUFFERED A COMPLICATION DUE TO THE CANNULA SHOOTING OFF INTO THE EYE WHILE HYDRATING PARACENTESIS AT THE END OF THE CASE. THE CANNULA DAMAGED CAPSULE AND ZONULES, CAUSING IOL(INTRAOCULAR LENS)/BAG COMPLEX TO DISLOCATE. THE IOL IMPLANT WAS CUT OUT OF THE EYE AND AN ANTERIOR VITRECTOMY WAS PERFORMED. THE PATIENT WAS LEFT APHAKIC. THE INITIAL INVESTIGATION FOLLOWING THIS EVENT DETERMINED THAT THE EVENT WAS DUE TO USER ERROR. HOWE
Patient problems: Eye Injury; Foreign Body In Patient
MAUDE report 17575795 ↗
Other Syringe, Piston devices
- BD Luer-Lok 309657Becton, Dickinson And Company · Syringe, piston1,266 reports
- BD Luer-Lok 309653Becton, Dickinson And Company · Syringe, piston948 reports
- BD Luer-Lok 309628Becton, Dickinson And Company · Syringe, piston862 reports
- N/A 302995Becton, Dickinson And Company · Syringe, piston1 recall537 reports
- BD Plastipak Syringe 300865Becton, Dickinson And Company · Syringe, piston515 reports
- N/A 302830Becton, Dickinson And Company · Syringe, piston462 reports
- N/A 302832Becton, Dickinson And Company · Syringe, piston424 reports
- BD Ultra-Fine 328468Becton, Dickinson and Company Inc · Syringe, piston323 reports
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.
How reports and recalls are matched · Editorial policy · Report an error on this page