{
  "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": "Plymouth",
      "address_1": "13355 10th Ave N",
      "reason_for_recall": "Laser Peripherals LLC  is recalling  DBLF-60-2 Bare Laser due to a mislabeling that indicated a sterility expiration date as '2016-16' as opposed to the intended date of '2016-06'.",
      "address_2": "Suite 110",
      "product_quantity": "25",
      "code_info": "E14128 & E14129",
      "center_classification_date": "20140717",
      "distribution_pattern": "Nationwide Distribution to IL, IN, and MD",
      "state": "MN",
      "product_description": "LP,Surgical Fibers,  Bare Laser Fiber 600 micron, DBLF-60-2, Sterile EO.    Laser surgical instrument for use in general and plastic surgery and in dermatology",
      "report_date": "20140723",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Laser Peripherals LLC",
      "recall_number": "Z-2073-2014",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "68674",
      "termination_date": "20141022",
      "recall_initiation_date": "20140620",
      "postal_code": "55441-5553",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}