{
  "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": "2026-05-06",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Neuville Sur Oise",
      "state": "",
      "country": "France",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79269",
      "recalling_firm": "Hyphen BioMed",
      "address_1": "155 rue d Eragny",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide Distribution - US Distribution and to the countries of : Austria and France.",
      "recall_number": "Z-1062-2018",
      "product_description": "ZYMUTEST HIA IgGAM.   Model Number: RK040D.  Qualitative screening assay for the detection of heparin-dependent antibodies (IgG, IgM and IgA isotypes by ELISA. 96 Tests.",
      "product_quantity": "94",
      "reason_for_recall": "A voluntary recall is initiated for ZYMUTEST HIA lgGAM - Ref RK040D - Lot F1700415   and ZYMUTEST HIA MonoStrip lgGAM - Ref RK041D - Lot F1700416 because they may produce false positive results.",
      "recall_initiation_date": "20111109",
      "center_classification_date": "20180315",
      "termination_date": "20180621",
      "report_date": "20180321",
      "code_info": "UDI: 03663537018770  Lot Number: F1700415",
      "more_code_info": ""
    }
  ]
}