{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Portage",
      "address_1": "3800 E Centre Ave",
      "reason_for_recall": "It was identified that the Mistral-Air Premium blankets may be capable of  conducting electricity during a defibrillation or cardioversion therapy at higher  energy levels (70 Joules or more) when the blanket is applied with the reflective  side toward the patient (upside down).",
      "address_2": "",
      "product_quantity": "11160",
      "code_info": "LOT #(s):   1640002, 1645003",
      "center_classification_date": "20180127",
      "distribution_pattern": "U.S.",
      "state": "MI",
      "product_description": "MA3320-PM Premium Adult - SYK Mistral-Air Premium Blankets. MODEL #: MA3302-PM. CATALOG #(s): MA3302-PM",
      "report_date": "20180207",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Stryker Medical Division of Stryker Corporation",
      "recall_number": "Z-0419-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "78886",
      "termination_date": "20180322",
      "more_code_info": "",
      "recall_initiation_date": "20170721",
      "postal_code": "49002-5826",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}