Philips Bridge Prep Kit Recall: Catheter Resistance Risk

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Contact the company & request your remedy

Recalling firmMerit Medical Systems, Inc.1600 W Merit Pkwy · South Jordan, UT 84095-2416

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Philips is recalling its Bridge Prep Kit (REF K12-0:09098C) because the catheter may resist advancing over the guidewire. This could lead to complications during medical procedures if not handled properly.

Why it’s dangerous

The catheter may resist advancing over the guidewire during medical procedures. This resistance could cause complications like difficulty in procedure completion or potential injury to the patient.

Who’s affected

Healthcare professionals using the Bridge Prep Kit for medical procedures are most likely affected. Patients receiving this kit during procedures may also be impacted if the catheter resistance causes issues.

How to tell if you have this one

Check for the product name 'Bridge Prep Kit' with reference number K12-09098C. The kit is sterile and intended for medical use only. Affected units have specific lot numbers starting with 00884450024140.

Brand
Philips
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Verify the product name and reference number on the kit to confirm it matches the recalled model.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The recall indicates a potential risk during use, but the product is designed for medical procedures. Users should follow the recall instructions to ensure safety.

What should I do if I have this product?

The recall does not specify a remedy, so users should check the product details and contact Philips for further guidance.

How can I tell if my product is affected?

Affected units have the reference number K12-09098C and lot numbers starting with 00884450024140.

Take action

Contact Philips

We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-2004-2026 — Philips Philips

Hello,

I own a Philips that is covered by recall Z-2004-2026 from Philips.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-2004-2026 (April 2, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2004-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Merit Medical Systems, Inc. recalls Philips Bridge Prep Kit REF: K12-09098C Sterile EO, Rx ONLY

Lower-risk recall