Skip to content
Consumer Product Recalls
FDA2ActiveInternational

Z-2517-2026 โ€” Merit Medical Systems, Inc.

Announced
May 8, 2026
Published
Jun 18, 2026
Recall ID
98818
Lifecycle
Ongoing

Reason for recall

Due to unsealed portions of pouches.

Products (1)

  • 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.

Firms (1)

Distribution

States: 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, PR, RI, SC, TN, TX, UT, VA, WA, WI

Countries (foreign): AT, BE, CH, CZ, DE, DK, ES, FI, FR, GR, GT, IE, IT, KE, KZ, NL, NO, PT, SE