{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Marietta",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83465",
      "recalling_firm": "Owen Mumford USA, Inc.",
      "address_1": "1755 W Oak Commons Ct",
      "address_2": "N/A",
      "postal_code": "30062-2280",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "FL, LA, SC, CA, NJ, TX, NC, CO, NH, KY, NY, MO, PA",
      "recall_number": "Z-0263-2020",
      "product_description": "Autoject EI, REF AJ1310",
      "product_quantity": "1510 units",
      "reason_for_recall": "There is a possible assembly error on Autoject EI, lot number V14.  This lot was packed into two products: AJ 1310, lot number V14 and AN 3310VET (branded as Petfine Auto Injector), batches V14.V976 & V14.W107",
      "recall_initiation_date": "20190717",
      "center_classification_date": "20191101",
      "report_date": "20191113",
      "code_info": "Lot/Unit Number:  V14"
    }
  ]
}