Skip to the content

FDA Medical Device Recalls (openFDA)

Merit Medical Systems, Inc.: 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.

Recall number
Z-0060-2025
Recalling firm
Merit Medical Systems, Inc.
Product
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.
Status
Open, Classified
Initiated
2024-08-30
Posted
2024-10-11
Terminated
not on file
Reason
Due to a manufacturing process resulting in holes/breaches in the Tyvek sterile barrier.
Root cause
Nonconforming Material/Component
Action
On 08/30/2024, the firm email and/or UPS overnight delivery an "URGENT MEDICAL DEVICE RECALL NOTICE" informing customers that specific lots of MONARCH Inflation Devices due to a packaging defect, there may be a small hole in the Tyvek sterile barrier of the device packaging. Use of the affected product may result in exposure to pathogens/pyrogens which could lead to infection. Customer are instructed to: 1. Please immediately determine if any of the devices identified in the attached Customer Response Form (CRF) are within your facility, quarantine them, and discontinue use and distribution. 2. Ensure that applicable personnel within your organization are made aware of this field action. 3. If the product has been further distributed to other facilities, institutions, or manufacturers, please ensure this notice is immediately shared with them and note the quantity distributed on the CRF. Additional distribution details may be required by health authorities. 4. Please fill out, scan, and email the completed CRF to Customer Service at response@merit.com within 7 calendar days. All affected product shipped to you must be accounted for on the CRF. 5. Please immediately return all affected lots in your possession to Merit, per the instructions in the attached CRF. For questions - contact your Merit Sales Representative or Merit Customer Service via email at RESPONSE@merit.com or via phone at +1 800 356 3748 | Hours: 6 am to 6 pm MST | Mon-Fri.
Quantity
6,565 devices
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.
Lot, serial or model codes
Catalog Number: IN2430/B UDI-DI code: 00884450298053 Lot Number: H2298615 H2305035 H2309343 H2320982 H2326310 H2353508 H2369554 H2385820 H2395793 H2398305 H2413092 H2416388 H2421988 H2426107 H2432428 H2435884 H2442968 H2446110 H2453676 H2457934 H2462756 H2466450 H2478394 H2486953 H2492841 H2497956 H2507120 H2517518 H2522878 H2528487 H2540012 H2545411 H2554635 H2568222 H2574049 H2579554 H2584201 H2589843 H2594941 H2599815 H2614054 H2618904 H2622809 H2633299 H2639296 H2645647 H2649894 H2655507 H2660062 H2664663 H2669780 H2673558 H2697508 H2713941 H2733075 H2746745 H2751196 H2765642 H2806015 H2815182 H2819813 H2834412 H2842698 H2849884 H2861491 H2907143 H2918428
510(k) numbers
["K011811"]
PMA numbers
not on file
Product code
DXT
Firm FEI
1721504
Firm city
South Jordan
Firm state
UT
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

Search this register