{
  "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,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Guilford",
      "address_1": "741 Boston Post Rd",
      "reason_for_recall": "A component issue may cause the AED to abort a shock delivery or reset unexpectedly, which may cause an affected device to fail to delivery shock, and/or to fail to deliver shock in range.",
      "address_2": "Suite 201",
      "product_quantity": "860",
      "code_info": "Serial numbers:  400101347  400101348  400101350  400101351  400101364  400101365  400101368  400101371  400101373  400101380  400101381  400101382  400101384  400101385  400101390  400101392  400101395  400101396  400101398  400101399  400101400  400101401  400101402  400101403  400101404  400101405  400101406  400101407  400101408  400101409  400101410  400101411  400101412  400101413  400101414  400101415  400101418  400101419  400101420  400101421  400101422  400101423  400101424  400101425  400101427  400101428  400101429  400101430  400101431  400101432  400101433  400101434  400101435  400101436  400101437  400101438  400101439  400101441  400101442  400101444  400101446  400101447  400101448  400101449  400101451  400101452  400101453  400101454  400101455  400101456  400101457  400101458  400101459  400101460  400101461  400101462  400101463  400101464  400101465  400101466  400101467  400101468  400101469  400101470  400101471  400101472  400101473  400101474  400101475  400101477  400101478  400101480  400101483  400101486",
      "center_classification_date": "20200617",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution and the countries of Australia, Canada, France, Malaysia, Mauritius, Netherlands, Thailand, United Arab Emirates.",
      "state": "CT",
      "product_description": "DDU-2450 Lifeline ECG    Model Numbers DDU-A2450EN  DDU-E2450DE  DDU-E2450EN  DDU-E2450FR  DDU-E2450TH    Cat. No. DCF-A2460EN  DCF-A2463EN  DCF-E2460DE  DCF-E2460EN  DCF-E2460FR  DCF-E2460TH    UDI 00815098020287,  00815098020317  Automated External Defibrillators (AED) are indicated for use on victims of sudden cardiac arrest (SCA) who are: - unconscious and unresponsive, not breathing or not breathing normally.",
      "report_date": "20200624",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Defibtech, LLC",
      "recall_number": "Z-2394-2020",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "85702",
      "termination_date": "20210108",
      "more_code_info": "",
      "recall_initiation_date": "20200427",
      "postal_code": "06437-2714",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}