{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
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  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Center Valley",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92575",
      "recalling_firm": "Aesculap Implant Systems LLC",
      "address_1": "3773 Corporate Pkwy",
      "address_2": "N/A",
      "postal_code": "18034-8217",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of DC, MO, PA, TX.",
      "recall_number": "Z-2146-2023",
      "product_description": "Aesculap Surgical Needle, straight, 3 1/2\", (90 mm), 13GA, width: 2,400 mm, non-sterile, reusable  Article Number: MD610",
      "product_quantity": "7 units",
      "reason_for_recall": "Incorrect product code marked on the product, etched with product code MD611, however; the correct product code is MD610.",
      "recall_initiation_date": "20230518",
      "center_classification_date": "20230714",
      "report_date": "20230726",
      "code_info": "GUIDID: 04046963469054 Lot Number: 22002834",
      "more_code_info": ""
    }
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}