{
  "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,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Morrisville",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91312",
      "recalling_firm": "TELEFLEX LLC",
      "address_1": "3015 Carrington Mill Blvd",
      "address_2": "",
      "postal_code": "27560-5437",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic distribution to IL, MS, PA, TN.",
      "recall_number": "Z-0772-2023",
      "product_description": "Pilling Wecksorb Cylindrical Sponges",
      "product_quantity": "1,000 units",
      "reason_for_recall": "Specific lots have not been irradiated to eliminate pyronema and therefore the sterility of the affected products may be compromised.",
      "recall_initiation_date": "20220928",
      "center_classification_date": "20221228",
      "report_date": "20230104",
      "code_info": "Catalog Number: 200400, Lot Number: 22B0395",
      "more_code_info": ""
    }
  ]
}