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

Class II
Recalling firm
Merit Medical Systems, Inc.
Reason for recall
catheter may experience resistance when being advanced over the guidewire
Affected products (lot / model / serial)
All Lot Numbers/UDI: 00884450771310
Distribution pattern
US Nationwide distribution in the state of CO.
Firm location
South Jordan, UT, United States
Recall type
Voluntary: Firm initiated
How the firm notified customers
Letter
Product type
Devices
Status
Ongoing
Recall number
Z-2002-2026
Recall initiated
April 2, 2026
FDA classification date
April 29, 2026
FDA report date
May 6, 2026
FDA event ID
98637
Last updated on HTM Vibe
July 24, 2026
View on openFDA