Reported Oct 23, 2024 · Ongoing
Monarch Inflation Device 30 atm/bar REF IN2130 Injector And Syringe, Angiographic/Syringe, Balloon Inflation - The 30…
Merit Medical Systems, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Merit Medical Systems, Inc. · 1600 W Merit Pkwy · South Jordan, UT · 84095-2416
Is this the product you have?
- Monarch Inflation Device 30 atm/bar REF IN2130 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 codes and dates
- Catalog NumberIN2130/B
- UDI-DI code00884450298022
- Lot Number
127 of 127 codes
H2298616H2305036H2309344H2320983H2326311H2331539H2337133H2343847H2348708H2353509H2360153H2363096H2369555H2379873H2385821H2385822H2390615H2395794H2398306H2398307H2413093H2416389H2421990H2426109H2426110H2432438H2435891H2435892H2443005H2443006H2446111H2446112H2453677H2457935H2457936H2462761H2466451H2474178H2474381H2478395H2483315H2486954H2492842H2497958H2503845H2507121H2511931H2517519H2522879H2528488H2534959H2540013H2545412H2550517H2554636H2560207H2564558H2568223H2574050H2579555
- H2982494 H3000024 Catalog NumberIN2130/JPB
- UDI-DI code00884450298022
- Lot Number
H2298077H2311498H2318440H2326018H2335950H2348220H2361952H2378902H2397943H2446311H2457899H2466518H2511623H2538830H2617878H2632026H2645098H2709628H2721346H2739491H2746832H2756147H2765723H2770192H2790666H2799040H2806169
- H2838478 H2845266 Catalog NumberK05-02130
- UDI-DI code00884450047248
- Lot Number
H2304639H2326198H2353301H2360131H2412972H2443283H2454607H2473435H2503267H2516468H2673631H2708526H2751266H2756101H2856665
- Amount recalled
- 110,650 devices
This recall covers 16 products
The agency filed one notice per product. You are reading one of them; the other 15 are below.
3 more are in the archive.
Where it was sold
Why it was recalled
Due to a manufacturing process resulting in holes/breaches in the Tyvek sterile barrier.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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