# FDA recall Z-2517-2026

> **Merit Medical Systems, Inc.** · Class II · device recall initiated 2026-05-08.

## Product

Splashwire Hydrophilic Guide Wire:  REF: MSWSTDA35150  UDI-DI codes:  00884450529645  00884450529669  00884450529690    REF: MSWSTDA35180  UDI-DI codes:  00884450529645  00884450529669    REF: MSWSTDA35260EX  UDI-DI code:  00884450529683    REF: MSWSTDA3580  UDI-DI codes:  00884450529645  00884450529690  00884450529744    REF: MSWSTDS35150  UDI-DI codes:  00884450529690  00884450529744    REF: MSWSTFA35260EX  UDI-DI code:  00884450529447    REF: MSWSTFA3580  UDI-DI code:  00884450529515    REF: MSWSTFS35150  UDI-DI code:  00884450529553    The Merit Hydrophilic Guide Wire is intended to be used in the peripheral vascular system to facilitate the placement of devices during diagnostic and interventional procedures.

## Reason for recall

Due to unsealed portions of pouches.

## Distribution

Worldwide - U.S. Nationwide distribution in the states and territory AL, AZ, CA, FL, GA, IA, ID, IL, IN, KS, MA, MD, ME, MI, MN, MO, MS, NC, NH, NJ, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, and Puerto Rico. The countries of Austria, Belgium, Czech Republic, Denmark, Finland, France, Germany, Greece, Guatemala, Ireland, Italy, Kazakhstan, Kenya, Netherlands, Norway, Portugal, Spain, Sweden, and Switzerland.

## Key facts

- **Recall number:** Z-2517-2026
- **Recalling firm:** Merit Medical Systems, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-05-08
- **Report date:** 2026-06-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** South Jordan, UT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2517-2026

## Citation

> MORVS. FDA recall Z-2517-2026. Retrieved 2026-10-18 from https://api.morvs.ai/recall/Z-2517-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*