{
  "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": [
    {
      "country": "United States",
      "city": "Greenville",
      "address_1": "10162 Bradford Rd",
      "reason_for_recall": "Device was distributed without a proper marketing authorization. This event is an expansion of RES 87581, Z-1355-2021 thru Z-1364-2021.",
      "address_2": "",
      "product_quantity": "Unknown",
      "code_info": "All lots sold prior to December 9, 2019.",
      "center_classification_date": "20210802",
      "distribution_pattern": "Worldwide distribution.",
      "state": "IN",
      "product_description": "TenderNeeds Fertility PRO IUI Human Artificial Home Insemination Kits, SKU 133166055771",
      "report_date": "20210811",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Tenderneeds Fertility LLC",
      "recall_number": "Z-2180-2021",
      "initial_firm_notification": "Other",
      "product_type": "Devices",
      "event_id": "88225",
      "more_code_info": "",
      "recall_initiation_date": "20201223",
      "postal_code": "47124-9227",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}