{
  "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": "2026-04-01",
    "results": {
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      "status": "Ongoing",
      "city": "Beaumont",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90060",
      "recalling_firm": "Helena Laboratories, Corp.",
      "address_1": "1530 Lindbergh Dr",
      "address_2": "",
      "postal_code": "77707-4131",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.: FL, MO, OH, and TX    O.U.S.: Canada, Uruguay, and Vietnam,",
      "recall_number": "Z-1244-2022",
      "product_description": "V8 Immunodisplacement Kit REF 1803",
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      "reason_for_recall": "Due to microbial growth causing interference with interpretation.",
      "recall_initiation_date": "20220406",
      "center_classification_date": "20220607",
      "report_date": "20220615",
      "code_info": "Model Number: 1803  UDI Codes:  +M52518030/SS73-21-1803/14D20230831Z  +M52518030/SS71-21-1803/14D20230830X  Lot 3-21-1803  Lot 1-22-1803",
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}