{
  "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": "Terminated",
      "city": "Greenville",
      "state": "SC",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85630",
      "recalling_firm": "PerkinElmer Health Sciences, Inc.",
      "address_1": "17 P & N Drive",
      "address_2": "N/A",
      "postal_code": "29611",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US  distribution in the state of Ohio",
      "recall_number": "Z-2264-2020",
      "product_description": "PerkinElmer 226 Sample Collection Device",
      "product_quantity": "164,952 devices",
      "reason_for_recall": "PerkinElmer 226 Sample Collection Devices Lot Number 40020001 had serial numbers printed on the pack labels that did not match the serial number range of the devices contained within the pack.",
      "recall_initiation_date": "20171219",
      "center_classification_date": "20200604",
      "termination_date": "20210326",
      "report_date": "20200610",
      "code_info": "UDI:  (01)50812589020011(17)200831(10)40020001; Serial Numbers:  06879601-06879700"
    }
  ]
}