{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "149335",
      "product_res_number": "Z-0319-2017",
      "event_date_initiated": "2016-08-30",
      "event_date_created": "2016-10-27",
      "recall_status": "Terminated",
      "event_date_terminated": "2018-06-07",
      "res_event_number": "75090",
      "product_code": "LKQ",
      "k_numbers": [
        "K100433"
      ],
      "product_description": "IMMULITE/ IMMULITE 1000 Systems CMM CMV IgM Assay, REF/Catalog Number LKCM1(D) - 100 tests (US), Siemens Material Number (SMN) 10370301 (US), Unique Device Identification Number (UDI) 00630414985718 (US); and  REF/Catalog Number LKCM1 - 100 tests (OUS); SMN 10381296 (OUS), UDI 00630414963747 (OUS); IVD --- Made in UK Siemens Healthcare Diagnostics Products Ltd., Glyn Rhonwy, Llanberis, Gwynedd, LL55 4EL UK\n\nFor in vitro diagnostic use with the IMMULITE Systems Analyzers for the qualitative detection of IgM antibodies to Cytomegalovirus (CMV) in human serum or plasma (EDTA or heparinized), as an aid in the determination of an acute CMV infection.",
      "code_info": "UDI 00630414985718/Catalog # LKCM1(D): Kit lot D0330;  UDI 00630414963747/Catalog # LKCM1: Kit lots 0330, 0331",
      "firm_fei_number": "2432235",
      "recalling_firm": "Siemens Healthcare Diagnostics, Inc.",
      "address_1": "511 Benedict Ave",
      "city": "Tarrytown",
      "state": "NY",
      "postal_code": "10591-5005",
      "reason_for_recall": "Multiple customers reported seeing an increase in imprecision with some patients resulting in high % CVs with the IMMULITE 2000/2000XPi CMV (IgM) assay starting with reagent lots 259 and above.",
      "root_cause_description": "Under Investigation by firm",
      "action": "The firm, Siemens, issued an \"Urgent Medical Device Recall\" Letter (IMC16-22.A.US, dated 8/30/2016) in the US and an \"Urgent Field Safety Notice\" (IMC16-22.A.OUS, dated August 2016) Outside the US (OUS) starting on 8/30/2016 The notices instructed customers to discontinue use of and discard the affected kit lots listed in the customer notice; review your inventory of the products to determine your laboratory's replacement needs; review the UMDR and or the UFSN with their Medical Director,  In the US, the method of distribution is FedEx and Outside the US the distribution is determined at the country level; complete and return the Field Correction Effectiveness Check Form via Fax to: Customer Care Center at (312) 275-7795 within 30 days, and retain this letter with your laboratory records, and forward this letter to those who may have received this product.\n\nIf you have any questions, please contact your Siemens Customer Care Center or your local Siemens technical support representative.",
      "product_quantity": "US: 5 kits; Foreign: 372 kits",
      "distribution_pattern": "Worldwide distribution- US (Nationwide) and countries of: United Arab Emirates, Afghanistan, Angola, Argentina, Australia, Bangladesh, Belgium, Bulgaria, Bahrain, Bolivia, Brazil, Belarus, Switzerland, Chile, China, Colombia, Costa Rica, Cyprus, Czech Republic, Germany, Dominican Republic, Algeria, Ecuador, Egypt, Spain, France, Great Britain, Greece, Guatemala, Honduras, Hungary, India, Iraq, Italy, Jordan, Canary Islands, Kyrgyzstan, Rep. Korea (S), Kazakhstan, Lebanon, Lithuania, Luxembourg, Latvia, Macedonia, Mexico, Malaysia, Nicaragua, Netherlands, Norway, Nepal, Peru, Pakistan, Poland, Portugal, Paraguay, Qatar, Romania, Russian Fed., Saudi Arabia, Singapore, Slovakia, El Salvador, Syria, Turkmenistan, Tunisia, Turkey, Uruguay, Uzbekistan, Vietnam, Serbia,and South Africa.",
      "openfda": {
        "k_number": [
          "K893465",
          "K853889",
          "K900743",
          "K913080",
          "K854839",
          "K872942",
          "K871832",
          "K861363",
          "K914789",
          "K972884",
          "K863798",
          "K922580",
          "K893466",
          "K831711",
          "K860450",
          "K872881",
          "K100433",
          "K933549"
        ],
        "registration_number": [
          "2915274",
          "3002806944",
          "2242436",
          "3005360469",
          "2432235",
          "1219913",
          "2029372",
          "8020790",
          "3007088335",
          "3032705"
        ],
        "fei_number": [
          "2915274",
          "3002806944",
          "2242436",
          "2432235",
          "3005670738",
          "1219913",
          "1220394",
          "1000306617",
          "1000611339",
          "3002701146"
        ],
        "device_name": "Antibody Igm,If, Cytomegalovirus Virus",
        "medical_specialty_description": "Microbiology",
        "regulation_number": "866.3175",
        "device_class": "2"
      }
    }
  ]
}