FDA recall record

Merit Medical Systems Monarch Inflation Device 30 atm/bar MAP403 MBA Hemostasis Valve Metal recall — FDA Z-0060-2025

Due to a manufacturing process resulting in holes/breaches in the Tyvek sterile barrier.

Class IIclassification
Z-0060-2025official record ID
Oct 23, 2024report date

Recall record at a glance

Official recordZ-0060-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmMerit Medical Systems, Inc.
Report dateOct 23, 2024
Recall initiation dateAug 30, 2024
Quantity6,565 devices
LocationSouth Jordan, UT, United States

Official product description

Monarch Inflation Device 30 atm/bar MAP403 MBA Hemostasis Valve Metal Insertion Tool Torque Device REF IN2430 Injector And Syringe, Angiographic/Syringe, Balloon Inflation - The 30 ATM Monarch syringe is used to inflate and deflate balloon angioplasty catheters and to measure the pressure within the balloon during the procedure. It is also used to inject fluids into the body and to monitor the pressure of that fluid.

Why the product was recalled

Due to a manufacturing process resulting in holes/breaches in the Tyvek sterile barrier.

Distribution information

Worldwide - U.S. Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, and WY. The countries of Belgium, Canada, France, Japan, Monaco, Netherlands, Qatar, United Arab Emirates, United Kingdom.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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About this record

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