FDA Class II · Medical device · June 24, 2026
Splashwire Hydrophilic Guide Wire recall — Merit Medical Systems, Inc.
Due to unsealed portions of pouches.
Official ID Z-2517-2026 · Official record ↗
Splashwire Hydrophilic Guide Wire: recall status
⚠ Recall found. Splashwire Hydrophilic Guide Wire is named in 1 official recall in our current data. Details and the official notices are below — act on the remedy in the official notice.
Recalls naming this model
See all Merit Medical Systems recalls →
Verify with the official sources:
- CPSC — consumer products ↗ (aggregated here)
- NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
- FDA — food, drugs, medical devices ↗ (aggregated here)
- USDA FSIS — meat, poultry & egg products ↗ (not yet aggregated here)
- Recalls.gov — the U.S. government’s all-agency portal ↗
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Compiled from official public-domain CPSC, NHTSA, and FDA data. Sources last checked July 24, 2026 at 1:12 AM UTC.