{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "109265",
      "product_res_number": "Z-0516-2013",
      "event_date_initiated": "2012-04-27",
      "event_date_posted": "2013-01-30",
      "recall_status": "Terminated",
      "event_date_terminated": "2018-06-29",
      "res_event_number": "61870",
      "product_code": "RFZ",
      "product_description": "Motorola Solutions  PCS3000/CS3070 Laser\n\nUtility/Peripheral Laser Products",
      "code_info": "Motorola Solutions  PCS3000/CS3070 Laser",
      "firm_fei_number": "3014423912",
      "recalling_firm": "Motorola Inc",
      "address_1": "1 Motorola Plz",
      "city": "Holtsville",
      "state": "NY",
      "postal_code": "11742-1300",
      "additional_info_contact": "Mr. Richard Blohm\n631-738-3474",
      "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.",
      "root_cause_description": "Radiation Control for Health and Safety Act",
      "action": "Motorola Solutions, Inc. agrees to provide instructions for downloading and installing a software update from the internet, which will reduce the laser power to IEC Class 1 AELs.  Purchasers will be provided an internet site and instructions for notifying Motorola Solutions, Inc. that the software installation and power reduction were successful, thereby completing the corrective action.\ncorrections to all units is anticipated to be completed by May 2013.\nI. Notifications to all dealers and purchasers must be made, and the FDA NY District Office Recall Coordinator is to be included in the notifications.  2.Correction of all units to be completed by May 2013.\n3.All products will be brought into compliance with the laser performance standard at no cost to the purchaser.  For questions regarding this recall call 631-738-3474.",
      "product_quantity": "16,961 units domestically",
      "distribution_pattern": "Nationwide distribution",
      "openfda": {
        "device_name": "Upc Scanner Reader (Bar Code Reader)",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "N"
      }
    }
  ]
}