Adelante Magnum ASM016035Recalls & reported problems
Oscor Inc. · Introducer Set with Hemostatic Valve, 16F · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885672004750), received between Oct 2, 2017 and Oct 2, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Difficult to Advance” (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 18, 2026.
Most reported problems
Device problems
- Difficult to Advance1
Patient problems
- Chronic Obstructive Pulmonary Disease (COPD)1
- High Blood Pressure/ Hypertension1
- Myocardial Infarction1
- Thrombus1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 2, 2017Difficult to Advance; Difficult to Advance
SURGEON WAS TRYING TO PUSH THE GUIDEWIRE AND OBTURATOR THROUGH THE SHEATH AND HAD DIFFICULTY PUSHING THEM THROUGH SHEATH. SURGEON TRIED A SECOND KIT BUT WAS AGAIN UNSUCCESSFUL. SURGEON AND OR STAFF OBTAINED ANOTHER INTRODUCER KIT FROM A DIFFERENT MANUFACTURER AND IT WAS SUCCESSFUL.
Patient problems: Chronic Obstructive Pulmonary Disease (COPD); High Blood Pressure/ Hypertension; Myocardial Infarction; Thrombus
MAUDE report 6909080 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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