PreludeSYNC™ 10884450286880Recalls & reported problems
Merit Medical Systems, Inc. · Class 2
All models of PreludeSYNC (4)
Data updated Oct 18, 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 10884450286880), received between Nov 26, 2025 and Nov 26, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Gas/Air Leak” (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.
Reports received per month
Most reported problems
Device problems
- Gas/Air Leak1
Patient problems
- Hematoma1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 26, 2025Gas/Air Leak; Gas/Air Leak
THE ACCOUNT ALLEGES THAT DURING A RADIAL ACCESS PROCEDURE, THE PHYSICIAN TRIED TO USE TWO DIFFERENT MERIT RADIAL COMPRESSION DEVICES. AIR WAS LEAKING BACK OUT OF THE DEVICE, AND THERE WAS NOT ENOUGH PRESSURE TO CLOSE THE RADIAL ARTERY ACCESS SITE. THE PATIENT DEVELOPED A LARGE HEMATOMA AND WAS ADMITTED OVERNIGHT FOR OBSERVATION.
Patient problems: Hematoma
MAUDE report 23658625 ↗
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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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