Drug recall
Philips Bridge Prep Kit REF: K12-09098B Sterile EO, Rx ONLY
FDA recall event 98637 · Class II · Merit Medical Systems, Inc.
Key facts
| Event ID | 98637 |
|---|---|
| Recall numbers | Z-2002-2026, Z-2003-2026, Z-2004-2026 |
| Recalling firm | Merit Medical Systems, Inc. |
| Product type | Devices |
| Products | Philips Bridge Prep Kit REF: K12-09098B Sterile EO, Rx ONLY, Philips Bridge Prep Kit REF: K12-09098C Sterile EO, Rx ONLY |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | catheter may experience resistance when being advanced over the guidewire |
| Initiation date | Apr 2, 2026 |
| Report date | May 6, 2026 |
| City | South Jordan |
| State | UT |
| Country | United States |
| FEI number | 1721504 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: