{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89855",
      "recalling_firm": "Hologic, Inc",
      "address_1": "10210 Genetic Center Dr",
      "address_2": "",
      "postal_code": "92121-4362",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: TX, TN, NY, NV, IN, AR, CA, CT, IL, NH, PA, WA, FL, OR, WV, VA, UT, MA, NJ, MI, PR  OUS: CA",
      "recall_number": "Z-0877-2022",
      "product_description": "Panther Fusion GBS Assay Cartridges 96 Tests, Catalog Number: PRD-04484.  in vitro diagnostic test for group b streptococcus.",
      "product_quantity": "2061",
      "reason_for_recall": "Samples, run on a GBS Assay, that have analyte concentrations that are at or near the limit of detection may produce false negative results.",
      "recall_initiation_date": "20220318",
      "center_classification_date": "20220406",
      "report_date": "20220413",
      "code_info": "UDI: 15420045510890, Lot numbers: 274954, 284599, 296991, 300796, 309230, 309353",
      "more_code_info": ""
    }
  ]
}