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: K12-0:09098B) because it may cause resistance when advancing catheters over guidewires. This could lead to complications during medical procedures.

Why it’s dangerous

The catheter may resist moving smoothly over the guidewire during medical procedures. This resistance could cause complications like kinks or delays in treatment.

Who’s affected

Healthcare professionals using the Bridge Prep Kit for medical procedures are most at risk. Patients receiving the kit are not directly affected.

How to tell if you have this one

Check for the product name 'Bridge Prep Kit' with reference number K12-09098B. The kit is sterile and intended for prescription use only. Lot numbers include 00884450771310.

Brand
Philips
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Identify the reference number K12-09098B and lot number 00884450771310 on the kit.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The recall indicates a potential risk of catheter resistance during use, but the product is still intended for medical procedures. Consult your healthcare provider for guidance.

What should I do if I have this product?

The recall does not specify a remedy, so contact Philips directly for further instructions.

How can I tell if I have the recalled product?

Look for the reference number K12-09098B and lot number 00884450771310 on the kit.

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-2002-2026 — Philips Philips

Hello,

I own a Philips that is covered by recall Z-2002-2026 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-2002-2026 (April 2, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2002-2026 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: K12-09098B Sterile EO, Rx ONLY

Lower-risk recall