Class II

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

Merit Medical Systems, Inc. · April 2, 2026

Reason for Recall

catheter may experience resistance when being advanced over the guidewire

Distribution

US Nationwide distribution in the state of CO.

States Affected

NATIONWIDE

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2002-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Merit Medical Systems, Inc. Medical Device Recall: Philips Bridge Prep Kit REF: K12-09098B Sterile EO, Rx ONLY | SafeCheck