{
  "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": "Kansas City",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94908",
      "recalling_firm": "American Contract Systems, Inc.",
      "address_1": "2610 Ne Industrial Dr Ste 220",
      "address_2": "",
      "postal_code": "64117-2648",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of CA, KS, ME, MN, MO, NE, and SD.",
      "recall_number": "Z-2518-2024",
      "product_description": "American Contract Systems Gyn Laparoscopy convenience kit",
      "product_quantity": "29 kits",
      "reason_for_recall": "Product released with insufficient aeration time impacting the kits sterilized on the same cycle or in the same aeration chamber, which may have been compromised in sterility",
      "recall_initiation_date": "20240506",
      "center_classification_date": "20240807",
      "report_date": "20240814",
      "code_info": "(1) Model No SLGL64K - UDI-DI 00191072202017; Lot 981241; Exp. Date 1/19/2025; and (2) Model No SMGY46A - UDI-DI 00191072188458; Lot 982241; Exp. Date 1/18/2025.",
      "more_code_info": ""
    }
  ]
}