{
  "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": "2026-04-15",
    "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": "77668",
      "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 to the state of : AL",
      "recall_number": "Z-2756-2017",
      "product_description": "PerkinElmer 226 Sample Collection Device    The PerkinElmer 226 Sample Collection Device is intended to be used as a medium to collect and transport whole blood specimen spots to a laboratory in Newborn Screening.",
      "product_quantity": "99,968 units",
      "reason_for_recall": "PerkinElmer 226 Sample Collection Devices Lot Number 317114 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": "20170531",
      "center_classification_date": "20170724",
      "termination_date": "20170727",
      "report_date": "20170802",
      "code_info": "lot numbers 317113 and 317114"
    }
  ]
}