{
  "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": "Ongoing",
      "city": "Greenville",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87581",
      "recalling_firm": "Tenderneeds Fertility LLC",
      "address_1": "10162 Bradford Rd",
      "address_2": "N/A",
      "postal_code": "47124-9227",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Other",
      "distribution_pattern": "World-wide distribution.",
      "recall_number": "Z-1355-2021",
      "product_description": "At Home Artificial Intrauterine Insemination Kit (SKU 636391205825, 636391205894, 636391205900, 636391205924, 636391205863, 636391205931, 636391205849, 636391206020, 644042787583, 636391205917, and 636391205801)",
      "product_quantity": "Unknown",
      "reason_for_recall": "Device was distributed without a proper marketing authorization.",
      "recall_initiation_date": "20201223",
      "center_classification_date": "20210406",
      "report_date": "20210414",
      "code_info": "All lots"
    }
  ]
}