Fresh Recalls

Merit Medical Systems recalls

5 recent recalls on record for Merit Medical Systems in connected official government data as of October 22, 2026 at 12:00 PM UTC.

Models with recalls

Embosphere 500-700 micrometer 2 mL Syringe Sterile Steam (1)Philips Bridge Prep Kit REF (3)Splashwire Hydrophilic Guide Wire (1)

All Merit Medical Systems recalls

FDA Class II · Medical device · October 7, 2026

Embosphere 500-700 micrometer 2 mL Syringe Sterile Steam recall — Merit Medical Systems, Inc.

Microspheres used in embolization of tumors, prostatic arteries, arteriovenous malformations, and blood vessels may have holes in packaging that may affect the sterile barrier, whi…

Official ID Z-3305-2026 · Official record ↗

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 ↗

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 ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 12:00 PM UTC.