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FDA (Device enforcement)Recalled 2024-08-30class ii

Merit Medical Systems, Inc.: Monarch Inflation Device 30 atm/bar MAP302 Honor Hemostasis Valve Metal Insertion Tool Torque Device REF IN2330 Injector And Syringe, Angiographic/Syringe, Balloon Inflati

Hazard

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

Details from the source

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. Quantity: 1,120 devices Lot/code info: Catalog Number: IN2330/B UDI-DI code: 00884450298046 Lot Number: H2369557 H2416390 H2421992 H2426112 H2492843 H2522880 H2540015 H2554505 H2560208 H2579556 H2765640 H2793109 H2806018 H2810777

UPC codes

00884450298046

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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