{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "175326",
      "product_res_number": "Z-0264-2020",
      "event_date_initiated": "2019-07-17",
      "event_date_created": "2019-11-01",
      "recall_status": "Open, Classified",
      "res_event_number": "83465",
      "product_code": "KZH",
      "k_numbers": [
        "K945660"
      ],
      "product_description": "Petfine Auto Injector, REF 3310VET",
      "code_info": "batches V14.V976 and V14.W107",
      "firm_fei_number": "1000219614",
      "recalling_firm": "Owen Mumford USA, Inc.",
      "address_1": "1755 W Oak Commons Ct",
      "city": "Marietta",
      "state": "GA",
      "postal_code": "30062-2280",
      "additional_info_contact": "Travis Shaw\n770-977-2226 Ext. 12",
      "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",
      "root_cause_description": "Employee error",
      "action": "The firm initiated the recall by letter on 07/17/2019.  The consignee was directed to quarantine all affected product and contact the company for return.  Distributors were also directed to cease distribution and contact their customers.",
      "product_quantity": "140 units",
      "distribution_pattern": "FL, LA, SC, CA, NJ, TX, NC, CO, NH, KY, NY, MO, PA",
      "openfda": {
        "k_number": [
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          "K033696",
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          "K141384",
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          "K060389",
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        ],
        "device_name": "Introducer, Syringe Needle",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.6920",
        "device_class": "2",
        "registration_number": [
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