{ "meta": { "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.", "terms": "https://open.fda.gov/terms/", "license": "https://open.fda.gov/license/", "last_updated": "2026-08-20", "results": { "skip": 0, "limit": 1, "total": 1 } }, "results": [ { "cfres_id": "192626", "product_res_number": "Z-0903-2022", "event_date_initiated": "2022-03-01", "event_date_created": "2022-04-11", "recall_status": "Open, Classified", "res_event_number": "89815", "product_code": "DTL", "product_description": "Access-9 Large Bore Hemostasis Valves, Catalog Code: 580775001, IN8112/C, K05-00053H, K05-00109G, K05-00137K, K05-00410G, K05-00438G, K05-00502F, K05-00587D, K05-01052, K05-01706C, K05-01880K, K05-02130, K05-02595, K09-12599A, K10-05487P, K12-00264, MAP111/F, MAP112/B, MAP112/F, K08-YP085A, K08-YS017B, K08-YS055A, K09-YS029A, K09-YS040F, K12-YP002A, K12-YP030A, K12-YP060A, K12-YP061A, K12-YP063C, K12-YP072, K12-YS018A, K12-YS019A, K12-YS026A, K05-01140D, K05-01706C***, K05-02595, MAP112, K05-00564L, K12-YP002A,", "code_info": "Catalog Code/Lots: \n580775001/I2219771, I2278741, I2226790;\nIN8112/C/H2292357, H2287440, H2281404, H2298626, H2305047, H2305048, H2309356;\nK05-00053H/H2305217;\nK05-00109G/H2304656;\nK05-00137K/H2304653;\nK05-00410G/H2305216;\nK05-00438G/H2309130;\nK05-00502F/H2309122;\nK05-00587D/H2309211;\nK05-01052/H2304607;\nK05-01706C/H2309133;\nK05-01880K/H2306962; \nK05-02130/H2304639;\nK05-02595/H2304614;\nK09-12599A/H2295450;\nK10-05487P/H2279857;\nK12-00264/H2285040;\nMAP111/F/I2259670, I2279884, I2259657, I2289610;\nMAP112/B/P1908667;\nMAP112/F/I2259661, I2279915, I2279894, I2176725, I2215955, I2289611, I2279895, I2289613, I2289612;\nK08-YP085A/H2249051, H2302394;\nK08-YS017B/H2249052;\nK08-YS055A/H2275990;\nK09-YS029A/H2266470, H2302474;\nK09-YS040F/H2286601;\nK12-YP002A/H2269321, H2278279, H2283742, H2295661;\nK12-YP030A/H2263653;\nK12-YP060A/H2272013;\nK12-YP061A/H2249088;\nK12-YP063C/H2272382, H2295556;\nK12-YP072/H2266224;\nK12-YS018A/H2284956;\nK12-YS019A/H2302506;\nK12-YS026A/H2276014, H2302507;\nK05-01140D/H2304611;\nK05-01706C/ (H2304610, H2309133)***;\nK05-02595/H2304614;\nMAP112/I2279895;\nK05-00564L/H2304617;\nK12-YP002A/H2295661;", "firm_fei_number": "1721504", "recalling_firm": "Merit Medical Systems, Inc.", "address_1": "1600 W Merit Pkwy", "city": "South Jordan", "state": "UT", "postal_code": "84095-2416", "additional_info_contact": "801-253-1600", "reason_for_recall": "A design change made to a hemostasis valve to improve manufacturability caused an internal gap between the rotator and the Y-body, where the guidewire can get caught, resulting in difficulty advancing the guidewire through the device. This defect may result in a delay of procedure.", "root_cause_description": "Component change control", "action": "On 03/01/22, recall notices were mailed to customers wo were informed to take the following actions:\n\n1. Quarantine and discontinue use, and distribution of affected devices.\n2. Ensure that applicable personnel within their organization are made aware of this field action.\n3. If the product has been further distributed to other facilities, institutions, or manufacturers, ensure the recall notice is immediately shared with them and note the quantity distributed on the Customer Response Form.\n4. Fill out, scan, and email the completed Customer Response Form to Customer Service at response@merit.com. All affected product shipped to you must be accounted for on the Customer Response Form.\n5. Immediately return all affected lots to the recalling firm.\n\nCustomers with additional questions are encouraged to contact a sales representative or the firm s customer service at RESPONSE-EMEA@merit.com, 1-800-356-3748, Hours: 6 am to 6 pm MST, Mon-Fri.\n\nRecall notices were also sent to Sales representatives who were asked to contact their affected accounts and assist with product return and completion of the Customer Response Form.\n\nOn 03/21/22, recall notices and response forms including an expanded scope were sent to customers informing them of additional distributed amounts of affected devices.", "product_quantity": "36445", "distribution_pattern": "US: MN, PA, AZ, FL, IL, AK, NY, CA, TX, KY, WI, NC, NJ, VA, CO, IN, AR, MO, LA, OR, MT, MA, MI, NE, WV, KS, MS, HI, IA, NH, ME, AL, DC, DE, NM, OH, GA, MD, TN, UT, RI, SC, OK, WA, ID, ND, SD, NV, VT.\n\nOUS: Poland, Germany, France, United Kingdom, Belgium, Korea, Republic of, Austria, Canada, Spain, Luxembourg, Italy, Switzerland, Czech Republic, Netherlands, Japan, Honduras, Colombia, Greece, Ireland", "openfda": { "k_number": [ "K791498", "K922840", "K870073", "K792113", "K961181", "K073474", "K993057", "K873971", "K122301", "K820297", "K954284", "K781579", "K033328", "K092563", "K854261", "K861783", "K760843", "K801200", "K092711", "K800880", "K831260", "K031398", "K812407", "K852118", "K801405", "K113845", "K945931", "K953564", "K772299", "K911884", "K862451", "K897137", "K073260", "K123448", "K884200", "K802544", "K040498", "K880831", "K892377", "K790564", "K840797", "K113148", "K860291", "K791914", "K873488", "K852086", "K072556", "K832625", "K893683", "K890580", "K872161", "K140475", "K902741", "K854397", "K910845", "K991102", "K853099", "K801402", "K812408", "K042060", "K863402", "K840603", "K934123", "K853749", "K780271", "K131124", "K791107", "K890676", "K854960", "K152528", "K820864", "K143429", "K912709", "K801399", "K093992", "K963749", "K870325", "K952531", "K897197", "K091634", 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"3005846326", "3002807314", "3002806469", "3002807111", "1625425", "3027637845", "3009291251", "3015276780", "2011171", "1000121056", "1718873", "2648727", "3007830707", "3010872792", "1000306431", "3003898360", "3008361782", "3004111573", "3045816907", "3011642792", "1048735", "3003945344", "3015309643", "2523676", "3002806565", "3006223010", "3004091615", "3012050423", "3010141307", "2521402", "2024024", "3004859241", "3012964172", "3018167761", "3012776242", "1018470", "1450662", "3004635528", "3010291427", "3009605245", "3004122598", "3017636737", "3008853977", "3002808467", "1000533027", "3008002401", "3005273623", "1625519", "3006942524", "3003932293", "3045058049", "3002534070", "1721504", "1043214", "3002913962", "1000112968", "3002963732", "1721676", "3007836437", "2024168", "3004194523", "3011237770", "3004961578", "3003737899", "1000512168", "3010188783", "3015173212", "1000112137", "3013557562", "3007835716", "3007361214", "3002808466", "3044778332", "3045816902", "3016950436", "1037885", "3038846851", "1820334", "3031571797", "3007289408", "3000717925", "3000335778", "3008403546", "1000117748", "3004605321", "3019807891", "1000112877", "3002806901", "1718850", "3036802499", "3011826338", "3033589330", "1643817", "3012536737", "3018312328", "3015910259", "3006210673", "3034544377", "3015225571", "3003094851", "1928237", "3003767881", "3022815697", "3006542380", "3008261722", "3010273872", "1000123180", "3031233007", "3000718472", "3005012805", "3006425876", "3009380063" ], "device_name": "Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass", "medical_specialty_description": "Cardiovascular", "regulation_number": "870.4290", "device_class": "2" } } ] }