{
  "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": "Center Valley",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68607",
      "recalling_firm": "Aesculap, Inc.",
      "address_1": "3773 Corporate Pkwy",
      "address_2": "",
      "postal_code": "18034-8217",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in the states of IL, NY, GA, and RI.",
      "recall_number": "Z-2024-2014",
      "product_description": "Dafilon Suture Black 10/0 (0.2) 15 cm DRM4 NS, non-sterile,  non-absorbable polyamide Surgical Suture, additional label affixed on the box states the product is sterile, packaged in a cassette holding 12 sutures",
      "product_quantity": "11",
      "reason_for_recall": "Aesculap Inc. (AIC (USA)) has initiated a voluntary recall of Dafilon Black 10/0 (0.2) 15 cm DRm4 non-sterile non-absorbable polyamide Surgical Suture due to a labeling issue.  Box labels do state non-sterile; however there is an additional label that is affixed on the box that states the product is sterile.",
      "recall_initiation_date": "20140613",
      "center_classification_date": "20140709",
      "termination_date": "20141007",
      "report_date": "20140716",
      "code_info": "Lot Numbers:  1-6375  1-8473  1-8433  1-9384  110054  110055",
      "more_code_info": ""
    }
  ]
}