{
  "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": [
    {
      "country": "United States",
      "city": "Allendale",
      "address_1": "110 Commerce Dr",
      "reason_for_recall": "There is a possibility that the product was packaged in the wrong  box. Specifically, the product may have been placed inside a BioMend box instead of a  BioMend Extend box. The only difference between the two boxes is the  product trade name. The label placed on the box and on the product packaged inside the box is  correct. The Instructions for Use inside the box are correct.",
      "address_2": "",
      "product_quantity": "569",
      "code_info": "CDMEN18F1, CDMEN18F3",
      "center_classification_date": "20181109",
      "distribution_pattern": "Distributed to one distributor located in Florida.",
      "state": "NJ",
      "product_description": "BioMend Extend, REF# 0142Z, Synthetic bone grafting material.",
      "report_date": "20181121",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Collagen Matrix, Inc.",
      "recall_number": "Z-0414-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "81282",
      "termination_date": "20200623",
      "more_code_info": "",
      "recall_initiation_date": "20180816",
      "postal_code": "07401-1622",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}