{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "Edison",
      "address_1": "125 May St Ste 300",
      "reason_for_recall": "Measurement listed on the label is not taken under tension, and this would cause possible extension of surgical time needed to complete the procedure.",
      "address_2": "",
      "product_quantity": "9 Qty",
      "code_info": "Serial #  00319004921075  00319004921073  00319007681048  00319014411085  00618052231059  03319006511040  03319009191029  03319019231072  03519018121056",
      "center_classification_date": "20190920",
      "distribution_pattern": "NY  NC  LA  TX  MO  OH",
      "state": "NJ",
      "product_description": "QuickGraft¿  Model # 430PST",
      "report_date": "20191002",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Musculoskeletal Transplant Foundation, Inc.",
      "recall_number": "Z-2548-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "83644",
      "termination_date": "20200701",
      "more_code_info": "",
      "recall_initiation_date": "20190815",
      "postal_code": "08837-3264",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}