FDAClass IIMay 6, 2026

Philips Bridge Prep Kit recall

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

Why was Philips Bridge Prep Kit recalled?

catheter may experience resistance when being advanced over the guidewire

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

All Lot Numbers/UDI: 00884450024140

Product
Philips Bridge Prep Kit REF: K12-09098C Sterile EO, Rx ONLY
Recalling firm
Merit Medical Systems, Inc.
Distribution
US Nationwide distribution in the state of CO.
Recall date
May 6, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls