{
  "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": {
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  "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-1363-2021",
      "product_description": "Pro Series Fertility Device (SKU 644042788139)",
      "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"
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}