{
  "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": "Bothell",
      "address_1": "22100 Bothell Everett Hwy",
      "reason_for_recall": "The recall is being initiated due to incorrect age range labeling (8+ yrs) on the foil packaging for infant/child pad cartridges. The infant/child pad cartridge is designed for use with the defibrillator An Infant/Child pad cartridge should not be used on an adult because it delivers lower energy (50 J vs 150 J) than the Adult pads cartridge and may therefore not be effective on an adult.",
      "address_2": "",
      "product_quantity": "181,894 Infant/Child SMART Pads  Pads",
      "code_info": "Model# M5072A; Lots #s Y070115-04 - Y011118-07;",
      "center_classification_date": "20190920",
      "distribution_pattern": "US: AK, AL,AR,AZ,CA,CO,CT,DE,FL,GA,HI,IA,ID,IL,IN,KS,KY,LA,MA,MD,ME,MI,MN,MO,MS,MT,NC,ND,NE,NH,NJ,NM,NV,NY,OH,OK,OR,PA,PR,RI,SC,SD,TN,TX,UT,VA,VT,WA,WI,WV, WY,    Argentina,  Aruba,  Australia,  Austria,  Belgium,  Bolivia,  Cambodia,  Canada,  Chile,  China,  Colombia,  Costa Rica,  Cyprus,  Denmark,  Dominican Republic,  Egypt,  El Salvador,  France,  French Guiana,  Germany,  Greece,  Guadeloupe,  Hong Kong,  India,  Indonesia,  Ireland,  Israel,  Italy,  Japan,  Korea, Republic of,  Malaysia,  Malta,  Martinique,  Mauritius,  Mexico,  Netherlands,  Netherlands Antilles,  New Caledonia,  New Zealand,  Norway,  Panama,  Paraguay,  Peru,  Philippines,  Poland,  Puerto Rico,  R¿union,  Singapore,  South Africa,  Spain,  Sweden,  Switzerland,  Taiwan,  Trinidad and Tobago,  United Arab Emirates,  United Kingdom,  Uruguay,  Viet Nam,",
      "state": "WA",
      "product_description": "Philips HeartStart Infant/Child SMART Pads Cartridge, Model # M5072A, UDI:00884838023758",
      "report_date": "20191002",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips North America LLC",
      "recall_number": "Z-2549-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "83681",
      "termination_date": "20210429",
      "more_code_info": "",
      "recall_initiation_date": "20180808",
      "postal_code": "98021-8431",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}