{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Irving",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "78225",
      "recalling_firm": "Abbott Laboratories, Inc",
      "address_1": "1921 Hurd Dr",
      "address_2": "N/A",
      "postal_code": "75038-4313",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution to US, Canada, France, and Germany.",
      "recall_number": "Z-0165-2018",
      "product_description": "ARCHITECT c4000 part number 02P24; ARCHITECT c8000 part number 01G06; ARCHITECT c16000 part number 03L77  Clinical Chemistry systems.",
      "product_quantity": "34 units",
      "reason_for_recall": "The Peristaltic Head tubing placed on the ARCHITECT c4000, c8000, and c16000  has the possibility to leak due to a manufacturing issue associated with the tubing connector.",
      "recall_initiation_date": "20170929",
      "center_classification_date": "20171121",
      "report_date": "20171129",
      "code_info": "c400073, c400103, c400498, c400600, c400890,  c400934, c400935, c401018, c401055, c401056,  c401182, c401505, c401520, c401686, c401887,  c460196, c460200, c460943, c461550, c803669, c803753, c1600144, c1600249, c1600251, c1600641, c1600720,  c1600819, c1600859, c1600976, c1601350, c1601351"
    }
  ]
}