{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Trumbull",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90782",
      "recalling_firm": "CooperSurgical, Inc.",
      "address_1": "95 Corporate Dr",
      "address_2": "N/A",
      "postal_code": "06611-1350",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic distribution to the following states: AL AZ CA CT DE FL GA HI IL KS MA MI MN MO NJ NY OH OR SC TX VA VT WA WI WV  Foreign distribution to Barbados, Canada, Chile, Micronesia Federate, and Panama.",
      "recall_number": "Z-1823-2022",
      "product_description": "Humidifier bottle and syringe filter kit (6 count of each) for the BT37  Mark II Benchtop Incubator (AY200246)",
      "product_quantity": "5,182 kits",
      "reason_for_recall": "There is a potential breach to the sterile barrier containing the Humidifier Bottles due to the packaging of the filter box located inside the bottle packaging. Damage to the sterile barrier may result in use of an unsterilized device, which may cause contamination and degradation or loss of embryo during incubation.",
      "recall_initiation_date": "20220812",
      "center_classification_date": "20220928",
      "report_date": "20221005",
      "code_info": "Lot Numbers  18-1265 18-1268 18-1268 / G004639  G004637  G004638  G004639"
    }
  ]
}