{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Ontario",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78037",
      "recalling_firm": "Aaren Scientific Inc.",
      "address_1": "1040 S Vintage Ave Ste A",
      "address_2": "N/A",
      "postal_code": "91761-3631",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide distribution including Puerto Rico.",
      "recall_number": "Z-0071-2018",
      "product_description": "AERO IOL Injection System containing 10  Z28 Cartridges per box, Part #003500-0025-282, Sterile, Rx.  The firm name on the label is Aaren Scientific Inc., Ontario, CA.  Used to fold and insert the firm's IOL's.",
      "product_quantity": "786 boxes",
      "reason_for_recall": "The recommended storage temperature on the label is incorrect.",
      "recall_initiation_date": "20170901",
      "center_classification_date": "20171108",
      "termination_date": "20180501",
      "report_date": "20171115",
      "code_info": "Lot numbers and expiration dates:  160204, 1/31/2018; 160505, 4/30/2018; 161006, 9/30/2018; 161018, 9/30/2018; 161028, 9/30/2018; 161219, 11/30/2018; and 170120, 12/31/2018."
    }
  ]
}