{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "cfres_id": "42988",
      "product_res_number": "Z-0321-06",
      "event_date_initiated": "2005-11-18",
      "event_date_posted": "2005-12-23",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-07-12",
      "res_event_number": "34045",
      "product_code": "MLN",
      "k_numbers": [
        "K003228"
      ],
      "product_description": "HeartStart  Pads Pediatric  Plus, Pediatric Plus Multifunction Defibrillation Electrode Pads\nModel M3717A",
      "code_info": "Lot Number : Y042005-1",
      "firm_fei_number": "1218950",
      "recalling_firm": "Philips Medical Systems",
      "address_1": "3000 Minuteman Road",
      "city": "Andover",
      "state": "MA",
      "postal_code": "01810-1032",
      "additional_info_contact": "Peter Ohanian\n978-659-4863",
      "reason_for_recall": "The Apex/Anterior and the Sternum/Posterior pad labels are located in reverse position to the wire and connector",
      "root_cause_description": "Other",
      "action": "Philips Medical sent the recall notification letter 11/30/05 via FedEx",
      "product_quantity": "253 CASES (5/CS)",
      "distribution_pattern": "Nationwide\nForeign:  Australia, Canada, France, germany, Spain,, Sweden, Switzerland, UK",
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        "device_name": "Electrode, Electrocardiograph, Multi-Function",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.2360",
        "device_class": "2"
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}