{
  "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,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "Berlin",
      "state": "N/A",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84716",
      "recalling_firm": "AAP Implantate Ag",
      "address_1": "Lorenzweg 5",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide Distribution",
      "recall_number": "Z-1675-2020",
      "product_description": "aap Implantate AG, Soft tissue retractor, radiolucent, REF IU 7971-00",
      "product_quantity": "7 units",
      "reason_for_recall": "The company has become aware that the soft tissue retractor is not always removed during the sawing process. This can result in damage to the soft tissue retractor in which abrasion debris can develop and remain in vivo.",
      "recall_initiation_date": "20191128",
      "center_classification_date": "20200406",
      "termination_date": "20250327",
      "report_date": "20200415",
      "code_info": "Lot Numbers:  I012, I025, I028"
    }
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}