{
  "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": "Terminated",
      "city": "Wayne",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82703",
      "recalling_firm": "Maquet Cardiovascular, LLC",
      "address_1": "45 Barbour Pond Dr",
      "address_2": "N/A",
      "postal_code": "07470-2094",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "Z-1581-2019",
      "product_description": "Maquet Getinge-BEQ-T 4903 Mercy Med w/o Oxy    Material:701066664",
      "product_quantity": "N/A",
      "reason_for_recall": "Custom Tubing Sets for Extracorporeal Circulation (ECC)-During sterilization, the closed stopcock/non-vented cap configuration may prevent the flow of humidity/ethylene oxide gas into the fluid-path between the closed port and the non-vented cap therefore the Sterility Assurance Level (SAL) of the stopcock ports cannot be assured",
      "recall_initiation_date": "20190418",
      "center_classification_date": "20190530",
      "termination_date": "20250728",
      "report_date": "20190605",
      "code_info": "Batch Numbers:   3000041468  3000053105  3000054552  3000057683  3000059795  3000065086  3000067186  3000069077  3000071375  3000072684  3000074341  3000075431  3000078942  3000080722  3000081524  3000084050"
    }
  ]
}