Impress® 00884450009185Recalls & reported problems
Merit Medical Systems, Inc. · Class 2
All models of Impress (145)
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 00884450009185), received between Jun 8, 2021 and Jun 8, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Fracture” (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
- Fracture1
- Material Separation1
Patient problems
- Coma1
- 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.
InjuryJun 8, 2021Fracture; Material Separation; Fracture; Material Separation
THE ACCOUNT ALLEGES THAT THE IMPRESS CATHETER TIP BROKE OFF DURING A NEUROLOGY VASCULAR INTERVENTION. THE TIP OF THE CATHETER MIGRATED ALONG THE VESSEL TOWARD THE BRAIN. THE PATIENT WAS UNCONSCIOUS AND COMATOSE. AN ADDITIONAL DEVICE WAS USED TO COMPLETE THE PROCEDURE.
Patient problems: Coma; Foreign Body In Patient
MAUDE report 11962101 ↗
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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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