{
  "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": "Waltham",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63771",
      "recalling_firm": "Perkinelmer",
      "address_1": "940 Winter Street",
      "address_2": "N/A",
      "postal_code": "02451",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide Distribution.",
      "recall_number": "Z-0689-2013",
      "product_description": "DBS MICROPLATE, TRUNCATED V-BOTTOMED  Product Number:        3033-0010",
      "product_quantity": "56  kits (100 plates/kit)",
      "reason_for_recall": "Truncated V-Bottomed Microplate Wells used in assays contain defective wells.",
      "recall_initiation_date": "20121126",
      "center_classification_date": "20130116",
      "termination_date": "20140307",
      "report_date": "20130123",
      "code_info": "Lot Numbers:    618609"
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}