Philips Bridge Prep Kit Recall: Catheter Resistance Risk

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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. Affected units have specific lot numbers.

Why it’s dangerous

The catheter may resist advancing over the guidewire during medical procedures. This could cause complications like procedure delays or incomplete treatments. The risk is low but requires careful handling.

Who’s affected

Healthcare professionals using the Bridge Prep Kit for medical procedures are most at risk. Patients receiving the kit during procedures may also be affected.

How to tell if you have this one

Check for the product name 'Bridge Prep Kit' with reference number K12-09098C. Affected units have specific lot numbers: 00884450816509.

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 packaging.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The recall indicates a potential risk, but the product is generally safe. Healthcare professionals should follow the recall instructions.

What should I do if I have this product?

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

How can I identify affected units?

Affected units have the lot number 00884450816509 and reference number K12-09098C.

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-2003-2026 — Philips Philips

Hello,

I own a Philips that is covered by recall Z-2003-2026 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-2003-2026 (April 2, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2003-2026 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