{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Holtsville",
      "address_1": "1 Motorola Plz",
      "reason_for_recall": "It was discovered the CS3000/CS3070  was manufactured using the laser power settings for a Class 2 laser device instead of the Class 1 power levels as specified on the product label.",
      "address_2": "",
      "product_quantity": "16,961 units domestically",
      "code_info": "Motorola Solutions  PCS3000/CS3070 Laser",
      "center_classification_date": "20130130",
      "distribution_pattern": "Nationwide distribution",
      "state": "NY",
      "product_description": "Motorola Solutions  PCS3000/CS3070 Laser    Utility/Peripheral Laser Products",
      "report_date": "20130206",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Motorola Inc",
      "recall_number": "Z-0516-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "61870",
      "termination_date": "20180629",
      "more_code_info": "",
      "recall_initiation_date": "20120427",
      "postal_code": "11742-1300",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}