{
  "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": "2026-07-08",
    "results": {
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      "city": "Indianapolis",
      "state": "IN",
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      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
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      "address_1": "9115 Hague Rd",
      "address_2": "",
      "postal_code": "46256-1025",
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      "product_description": "Creatine Kinase (CK) used on cobas c 311/501/502 and COBAS INTEGRA 400 plus-In vitro test for the quantitative determination of creatine kinase (CK) in human serum and plasma.  Catalog Number: 07190794190",
      "product_quantity": "6504 units",
      "reason_for_recall": "Creatine Kinase (CK) Assay Abnormal calibrations on the cobas¿ c 311/501/502 and COBAS INTEGRA 400 plus Analyzers may lead to erroneous results and misdiagnosis.",
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      "code_info": "UDI-DI: 04015630940806 Lot Number: 755471 Exp. Date: 06/30/2024",
      "more_code_info": ""
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}