Monarch Inflation Device 30 atm/bar MAP152 AssessPLUS Large Bore Hemostasis Valve Metal Insertion Tool Torque Device REF
Summary
The FDA issued a Class II for Monarch Inflation Device 30 atm/bar MAP152 AssessPLUS Large Bore Hemostasis Valv by Merit Medical Systems, Inc.. Reason: Due to a manufacturing process resulting in holes/breaches in the Tyvek sterile barrier..
Details
Source
Device Recall
External ID
Z-0061-2025
Action Date
2024-10-23
Status
Ongoing
Category
device
Product Description
Monarch Inflation Device 30 atm/bar MAP152 AssessPLUS Large Bore Hemostasis Valve Metal Insertion Tool Torque Device REF IN2530 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.
Lot/Code Info: Catalog Number: IN2530/B UDI-DI code: 00884450298060 Lot Number: H2305037 H2309345 H2312492 H2320984 H2326312 H2331540 H2337135 H2343848 H2348709 H2353510 H2379875 H2385823 H2398320 H2413098 H2416393 H2421995 H2426129 H2432439 H2435893 H2443007 H2446113 H2453678 H2457937 H2458275 H2466457 H2474179 H2483316 H2486955 H2492844 H2497959 H2503846 H2507122 H2511932 H2517520 H2522881 H2528489 H2534960 H2540016 H2545413 H2550521 H2554673 H2560209 H2564559 H2568225 H2574051 H2579557 H2584204 H2594880 H2594944 H2599817 H2604242 H2610526 H2614059 H2618906 H2622811 H2629607 H2633301 H2639298 H2645654 H2649898 H2655509 H2660065 H2664666 H2669781 H2672437 H2673582 H2683311 H2688025 H2693066 H2703591 H2713947 H2733076 H2746748 H2751197 H2760547 H2769987 H2774666 H2784537 H2789807 H2793110 H2801750 H2806027 H2810778 H2824764 H2834413 H2838430 H2845204 H2847853 H2849888 H2849889 H2856554 H2861492 H2867260 H2871518 H2880698 H2890797 H2907144 H2912644 H2918429 H2925194 H2929405 H2934699 H2937986 H2943479 H2978085 H2982496 H2989541 H2994311 H3000025 H3009570
Quantity Affected: 51,900 devices
Reason for Recall
Due to a manufacturing process resulting in holes/breaches in the Tyvek sterile barrier.
Distribution
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.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-08-30
Company
South Jordan, UT
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 180 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Merit Medical Systems, Inc. has 117 FDA actions in our database, including 95 recalls and 22 clearances.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Merit Medical Systems, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Merit Medical Systems, Inc. have FDA actions?
Merit Medical Systems, Inc. has 117 FDA actions in our database, including 95 recalls and 22 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-0061-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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