# FDA recall Z-2002-2026

> **Merit Medical Systems, Inc.** · Class II · device recall initiated 2026-04-02.

## Product

Philips Bridge Prep Kit  REF: K12-09098B  Sterile EO, Rx ONLY

## Reason for recall

catheter may experience resistance when being advanced over the guidewire

## Distribution

US Nationwide distribution in the state of CO.

## Key facts

- **Recall number:** Z-2002-2026
- **Recalling firm:** Merit Medical Systems, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-04-02
- **Report date:** 2026-05-06

- **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-2002-2026

## Citation

> AI Analytics. FDA recall Z-2002-2026. Retrieved 2026-06-01 from https://api.ai-analytics.org/recall/Z-2002-2026. Source: US FDA. Licensed CC0.

---

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