Hydrophilic Prelude SNAPRecalls & reported problems across all models
Merit Medical Systems, Inc. · 5 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one Hydrophilic Prelude SNAP model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 5 models of Hydrophilic Prelude SNAP by Merit Medical Systems, Inc. in the FDA's device registry (GUDID). Together they are named in 1 adverse event report in the FDA's MAUDE database, received between Aug 27, 2025 and Aug 27, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (1 report).
1 FDA recall record name at least one of these models by its device identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Hydrophilic Prelude SNAP recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Jun 11, 2024Open, Classified
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
Z-2575-2024 · Root cause: No Marketing Application · names 5 of these models · Recall details · FDA record ↗
Most reported Hydrophilic Prelude SNAP problems
Device problems
- Break1
- Fracture1
- Material Integrity Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Hydrophilic Prelude SNAP models
5 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Hydrophilic Prelude SNAP™ 10884450495046INTRODUCER, CATHETER1 recall1 report
- Hydrophilic Prelude SNAP™ 10884450495053INTRODUCER, CATHETER1 recall0 reports
- Hydrophilic Prelude SNAP™ 10884450495084INTRODUCER, CATHETER1 recall0 reports
- Hydrophilic Prelude SNAP™ 10884450495497INTRODUCER, CATHETER1 recall0 reports
- Hydrophilic Prelude SNAP™ 10884450495503INTRODUCER, CATHETER1 recall0 reports
Recent Hydrophilic Prelude SNAP adverse event reports
The 1 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionAug 27, 2025Break; Fracture; Material Integrity Problem; Break; Fracture; Material Integrity Problem
THE ACCOUNT ALLEGES THAT THEY ARE UNABLE TO TEAR AWAY THE SPLITABLE SHEATH. NO PATIENT INJURY TO REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22909982 ↗
Other Merit Medical Systems, Inc. products
- Aspira11 models · 36 reports · 10 recalls
- Impress145 models · 481 reports
- Monarch6 models · 37 reports · 7 recalls
- Bridge Prep Kit4 models · 6 reports · 3 recalls
- Prelude Roadster33 models · 1 reports · 3 recalls
- basixTOUCH6 models · 1 reports · 3 recalls
- basixCOMPAK34 models · 34 reports · 2 recalls
- Flex-Neck11 models · 21 reports · 2 recalls
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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