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 ↗
Merit Medical Systems recalls
4 recent recalls on record for Merit Medical Systems in CPSC, NHTSA, and FDA data as of July 24, 2026 at 1:12 AM UTC.
Models with recalls
All Merit Medical Systems recalls
FDA Class II · Medical device · May 6, 2026
Philips Bridge Prep Kit REF recall — Merit Medical Systems, Inc.
catheter may experience resistance when being advanced over the guidewire
Official ID Z-2004-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Philips Bridge Prep Kit REF recall — Merit Medical Systems, Inc.
catheter may experience resistance when being advanced over the guidewire
Official ID Z-2003-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Philips Bridge Prep Kit REF recall — Merit Medical Systems, Inc.
catheter may experience resistance when being advanced over the guidewire
Official ID Z-2002-2026 · Official record ↗
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 ↗
Found something wrong or missing? Report a data error.
Compiled from official public-domain government data. Last checked July 24, 2026 at 1:12 AM UTC.