{
  "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": "Andover",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89023",
      "recalling_firm": "Philips Healthcare",
      "address_1": "3000 Minuteman Rd",
      "address_2": "",
      "postal_code": "01810-1032",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-0241-2022",
      "product_description": "CombiDiagnost R90 is multi-functional general R/F systems.",
      "product_quantity": "281 in total",
      "reason_for_recall": "The Aleva monitor requires certain labels to be applied, some of which are required by FDA Electronic Product Radiation Control performance standards.  This includes the Radiation Warning Label [21CFR 1020.30 (j)] and the X-ray control certification  statement [21 CFR 1010.2]. Philips has determined that some systems at customer locations did not have these labels applied.",
      "recall_initiation_date": "20210922",
      "center_classification_date": "20211124",
      "report_date": "20211201",
      "code_info": "CombiDiagnost R90",
      "more_code_info": ""
    }
  ]
}