{
  "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": "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:  400086354  400086358  400090005  400091761  400093477  400093478  400093479  400093480  400093481  400093482  400093483  400093484  400093485  400093486  400093487  400093488  400093489  400093490  400093491  400093492  400093493  400093494  400093495  400093496  400093497  400093498  400093499  400093500  400093501  400093502  400093503  400093504  400093505  400093506  400093508  400093510  400093512  400093513  400093514  400093515  400093516  400093517  400093518  400093519  400093520  400093521  400093522  400093523  400093524  400093525  400093527  400093528  400093529  400093530  400093531  400093532  400093533  400093534  400093535  400093536  400093538  400093539  400093540  400093541  400093542  400093543  400093544  400093545  400093546  400093547  400093548  400093549  400093550  400093551  400093552  400093553  400093554  400093555  400093556  400093557  400094155  400098786  400098812  400101171  400101172  400101174  400101175  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      "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-2300 Lifeline/ReviveR View, Model Numbers DDU-C2300EN, DDU-C2300CA, DDU-A2300EN, DDU-E2300EN    Catalog Numbers CCD-A1006RX  CCD-A1013EN  CCD-A1015EN  DCF-A2310EN  DCF-A2310RX  DCF-A2313EN  DCF-C2310CA  DCF-C2310EN  DCF-E2310CA  DCF-E2310EN    UDI 00815098020201,  00815098020225, 00815098020232  Product Usage: 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-2392-2020",
      "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"
    }
  ]
}