United StatesPhilips Bridge Prep Kit REF: K12-09098B Sterile EO, Rx ONLY and Philips Bridge Prep Kit REF: K12-09098C Sterile EO, Rx ONLY (All Lot Numbers/UDI: 00884450771310, 00884450816509, 00884450024140) are affected. They were recalled because the catheter may experience resistance when being advanced over the guidewire; the kits were distributed in the state of CO in the United States.
What's being recalled
Philips Bridge Prep Kit REF: K12-09098B Sterile EO, Rx ONLY
Philips Bridge Prep Kit REF: K12-09098C Sterile EO, Rx ONLY
Recalling firm: Merit Medical Systems, Inc., South Jordan, UT, United States.
How to identify it
All Lot Numbers/UDI: 00884450771310 All Lot Numbers/UDI: 00884450816509 All Lot Numbers/UDI: 00884450024140
The hazard
catheter may experience resistance when being advanced over the guidewire
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
US Nationwide distribution in the state of CO.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)