{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Billerica",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90107",
      "recalling_firm": "PROTERIXBIO",
      "address_1": "1 Fortune Dr",
      "address_2": "N/A",
      "postal_code": "01821-3923",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Domestic distribution to CA CO FL IA MA MO NH NY OH OK TX VA",
      "recall_number": "Z-1058-2022",
      "product_description": "ProterixBio SARS-CoV-2 (RBD) IgG Antibody Test, and associated ProterixBio Dried Blood Spot Collection Kit, no model number",
      "product_quantity": "640 kits",
      "reason_for_recall": "FDA review concluded that the test is insufficiently supported by clinical performance data, and results reported may not have been accurate (false positives or false negatives).",
      "recall_initiation_date": "20220417",
      "center_classification_date": "20220511",
      "termination_date": "20240123",
      "report_date": "20220518",
      "code_info": "Lots were not coded. All product will be recalled."
    }
  ]
}