medical MODERATE Updated 2026-05-06

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

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Recalled Product

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

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Hazard / Issue

catheter may experience resistance when being advanced over the guidewire

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: All Lot Numbers/UDI: 00884450771310

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

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