{
  "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": "2026-04-22",
    "results": {
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  "results": [
    {
      "country": "United States",
      "city": "Hazelwood",
      "address_1": "595 Anglum Rd",
      "reason_for_recall": "The product package did not contain the correct version of the package insert listing the limitations of use and performance requirements.",
      "address_2": "",
      "product_quantity": "4/20-card cartons",
      "code_info": "lot number: 540274420",
      "center_classification_date": "20130327",
      "distribution_pattern": "Distributed only in HI.",
      "state": "MO",
      "product_description": "bioMerieux VITEK 2 AST-ST01 Streptococcus Susceptibility Card, REF 410 028.    For use with VITEK 2 systems to determine the susceptibility of Streptococcus to antimicrobial agents.",
      "report_date": "20130403",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Biomerieux Inc",
      "recall_number": "Z-1013-2013",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "64327",
      "termination_date": "20131030",
      "more_code_info": "",
      "recall_initiation_date": "20130206",
      "postal_code": "63042-2320",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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