- Recalling firm
- Merit Medical Systems, Inc.
- Reason for recall
- catheter may experience resistance when being advanced over the guidewire
- Affected products (lot / model / serial)
- All Lot Numbers/UDI: 00884450024140
- Distribution pattern
- US Nationwide distribution in the state of CO.
- Firm location
- South Jordan, UT, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2004-2026
- Recall initiated
- April 2, 2026
- FDA classification date
- April 29, 2026
- FDA report date
- May 6, 2026
- FDA event ID
- 98637
- Last updated on HTM Vibe
- July 24, 2026