{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Santa Ana",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93726",
      "recalling_firm": "Fujifilm Irvine Scientific, Inc.",
      "address_1": "2511 Daimler St",
      "address_2": "",
      "postal_code": "92705-5533",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: OK, CA, DC, NC, NV, TX, MI, IN, NY, UT, WI, MN, PA, WV, NJ, IL, LA, WA, OR, FL, IA.  OUS: GB, NL, AR, MY",
      "recall_number": "Z-0998-2024",
      "product_description": "Sperm separation media are used to separate motile sperm from other constituents of semen.",
      "product_quantity": "246",
      "reason_for_recall": "The lower layer component of a sperm separation Kit does not match the certificate of analysis. The kit should contain lower layer (Lot: 0000020686, Shelf Life: 31 December 2024) but incorrectly may contain lower layer (Lot number 9925811106, Shelf Life: 30 November 2023).",
      "recall_initiation_date": "20231102",
      "center_classification_date": "20240206",
      "report_date": "20240214",
      "code_info": "UDI-DI: 00857515006009, Lot 0000020693",
      "more_code_info": ""
    }
  ]
}