{
  "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": [
    {
      "country": "United States",
      "city": "Parsippany",
      "address_1": "5 Century Dr",
      "reason_for_recall": "There have been reports of shortened (T1-T2) results, where some instances of result recovery outside of the range of less than or equal to 15 seconds.",
      "address_2": "",
      "product_quantity": "22342 total",
      "code_info": "Lot #s 251918, 252751",
      "center_classification_date": "20181214",
      "distribution_pattern": "US Nationwide Distribution",
      "state": "NJ",
      "product_description": "Staclot¿ LA (REF 00600)     The Staclot¿ LA and Staclot¿ LA 20 test kits are reagent systems designed for the qualitative detection of lupus anticoagulants (LA) in plasma by the use of hexagonal HII phase phospholipid molecules (1, 2).",
      "report_date": "20181226",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Diagnostica Stago, Inc.",
      "recall_number": "Z-0610-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "81678",
      "termination_date": "20200608",
      "more_code_info": "",
      "recall_initiation_date": "20181114",
      "postal_code": "07054-4607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}