ImpressRecalls & reported problems across all models
Merit Medical Systems, Inc. · 145 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Impress models — page 2
145 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- Impress® 00884450042489CATHETER, INTRAVASCULAR, DIAGNOSTIC1 report
- Impress® 00884450042526CATHETER, INTRAVASCULAR, DIAGNOSTIC1 report
- Impress® 00884450042540CATHETER, INTRAVASCULAR, DIAGNOSTIC1 report
- Impress® 00884450042557CATHETER, INTRAVASCULAR, DIAGNOSTIC1 report
- Impress® 00884450043325CATHETER, INTRAVASCULAR, DIAGNOSTIC1 report
- Impress® 00884450043745CATHETER, INTRAVASCULAR, DIAGNOSTIC1 report
- Impress® 00884450103234CATHETER, INTRAVASCULAR, DIAGNOSTIC1 report
- Impress® 00884450113868CATHETER, INTRAVASCULAR, DIAGNOSTIC1 report
- Impress® 00884450169865CATHETER, INTRAVASCULAR, DIAGNOSTIC1 report
- Impress® 00884450273777CATHETER, INTRAVASCULAR, DIAGNOSTIC1 report
- Impress® 00884450295922CATHETER, INTRAVASCULAR, DIAGNOSTIC1 report
- Impress® 00884450646618Catheter, intravascular, diagnostic1 report
- Impress® 00884450653739Catheter, intravascular, diagnostic1 report
- Impress® 00884450654521Catheter, intravascular, diagnostic1 report
- Impress® 00884450654545Catheter, intravascular, diagnostic1 report
- Impress® 00884450661420Catheter, intravascular, diagnostic1 report
- Impress® 00884450661437Catheter, intravascular, diagnostic1 report
- Impress® 00884450661499Catheter, intravascular, diagnostic1 report
- Impress® 00884450661505Catheter, intravascular, diagnostic1 report
- Impress® 00884450661581Catheter, intravascular, diagnostic1 report
- Impress® 00884450668115Catheter, intravascular, diagnostic1 report
- Impress® 00884450668139Catheter, intravascular, diagnostic1 report
- Impress® 00884450668788Catheter, intravascular, diagnostic1 report
- Impress® 00884450668795Catheter, intravascular, diagnostic1 report
- Impress® 00884450677544Catheter, intravascular, diagnostic1 report
- Impress® 00884450683729Catheter, intravascular, diagnostic1 report
- Impress® 00884450683781Catheter, intravascular, diagnostic1 death1 report
- Impress® 00884450683842Catheter, intravascular, diagnostic1 report
- Impress® 00884450685433Catheter, intravascular, diagnostic1 report
- Impress® 00884450687376Catheter, intravascular, diagnostic1 report
- Impress® CCatheter, intravascular, diagnostic1 report
- Impress® 00884450697313Catheter, intravascular, diagnostic1 report
- Impress® 00884450709412Catheter, intravascular, diagnostic1 report
- Impress® 00884450712191Catheter, intravascular, diagnostic1 report
- Impress® 00884450712221Catheter, intravascular, diagnostic1 report
- Impress® 00884450717936Catheter, intravascular, diagnostic1 report
- Impress® 00884450717950Catheter, intravascular, diagnostic1 report
- Impress® CCatheter, intravascular, diagnostic1 report
- Impress® CCatheter, intravascular, diagnostic1 report
- Impress® BCatheter, intravascular, diagnostic1 report
- Impress® CCatheter, intravascular, diagnostic1 report
- Impress® CCatheter, intravascular, diagnostic1 report
- Impress® CCatheter, intravascular, diagnostic1 report
- Impress® CCatheter, intravascular, diagnostic1 report
- Impress® CCatheter, intravascular, diagnostic1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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.
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