{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Bedford",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98166",
      "recalling_firm": "Instrumentation Laboratory",
      "address_1": "180 Hartwell Rd",
      "address_2": "",
      "postal_code": "01730-2443",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of CA, FL, IL, MN, MS, NE, OH, TX, WI and the countries of Belgium, Netherlands, Luxembourg, Switzerland, China, Hong Kong, Israel, Italy, South Korea, Lithuania, Macao, Malaysia, Philippines, Qatar, Romania, Turkey, Kosovo.",
      "recall_number": "Z-1095-2026",
      "product_description": "The product is used for the evaluation of the intrinsic coagulation pathway, APTT substitution test and the monitoring of  heparin therapy.",
      "product_quantity": "7,720 units",
      "reason_for_recall": "Potential for microbial contamination.",
      "recall_initiation_date": "20251211",
      "center_classification_date": "20260115",
      "report_date": "20260121",
      "code_info": "Part Number: 0020006800.  UDI-DI:  08426950078920. Lot Number: N1136730.  Expiration Date 12/31/2025.",
      "more_code_info": ""
    }
  ]
}