{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Braintree",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70352",
      "recalling_firm": "Haemonetics Corporation",
      "address_1": "400 Wood Rd",
      "address_2": "",
      "postal_code": "02184-2412",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution -- US, Canada, Czech Republic, Denmark, Great Britain, and Sweden.",
      "recall_number": "Z-1130-2015",
      "product_description": "Haemonetics TEG Hemostasis System Level II Control,  Catalog number: 8002.    Level II Control is a biological control for use with the Thrombelastograph (TEG) Hemostasis System.",
      "product_quantity": "4,143 kits",
      "reason_for_recall": "Specific lots of Level II Control Kits produce high Maximum Amplitude (MA) results, which are outside of the manufacturer's expected Quality Control range for MA parameter.",
      "recall_initiation_date": "20150126",
      "center_classification_date": "20150219",
      "termination_date": "20150605",
      "report_date": "20150225",
      "code_info": "Lot numbers:  HMO 9200   HMO 9217   HMO 9226   HMO 9232   HMO 9276   HMO 9285   HMO 9292  Exp. Date 1/2017",
      "more_code_info": ""
    }
  ]
}