Merit Medical Systems, Inc. recalls Philips Bridge Prep Kit REF: K12-09098C Sterile EO
- Recalling company
- Merit Medical Systems, Inc.
- Product
- Philips Bridge Prep Kit REF: K12-09098C Sterile EO, Rx ONLY
- Reason
- catheter may experience resistance when being advanced over the guidewire
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Apr 2, 2026
- Reported
- May 6, 2026
- Distribution
- US Nationwide distribution in the state of CO.
- Status
- Ongoing
- Lot / codes
- All Lot Numbers/UDI: 00884450816509
- Company location
- South Jordan, UT
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2003-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2003-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.