{
  "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,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Rochester",
      "address_1": "1049 Ridge Rd W",
      "reason_for_recall": "Carestream DRX-1 System batteries manufactured before June 2012 due to two occurrences of lithium-ion battery overheating, which may cause burns.",
      "address_2": "",
      "product_quantity": "9971 units",
      "code_info": "All DRX-1 batteries manufactured before June 2012.",
      "center_classification_date": "20120813",
      "distribution_pattern": "Worldwide Distribution, including Nationwide (USA).",
      "state": "NY",
      "product_description": "Carestream DRX-1 System Battery --- Made in U.S.A. for Carestream Health, Inc., Carestream Health, Inc., 150 Verona St, Rochester, NY 14608. --- The battery may be sold with the DRX-1 imaging device or as a stand-alone accessory.",
      "report_date": "20120822",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Carestream Health, Inc.",
      "recall_number": "Z-2202-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "62310",
      "termination_date": "20160525",
      "more_code_info": "",
      "recall_initiation_date": "20120612",
      "postal_code": "14615-2731",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}