Official recall notice

FDA DeviceClass IINotable

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

Recall date
2026-05-06
FDA class
Class II

Why it was recalled

Hazard

catheter may experience resistance when being advanced over the guidewire

Product description

catheter may experience resistance when being advanced over the guidewire

Verify with the official notice →
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