{
  "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": "90962",
      "recalling_firm": "TELEFLEX LLC",
      "address_1": "3015 Carrington Mill Blvd",
      "address_2": "N/A",
      "postal_code": "27560-5437",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "TN, CA, NC, TX, FL, OH, MO, IL, OR",
      "recall_number": "Z-0227-2023",
      "product_description": "Teleflex Medical RUSCH Pocket Pac i.c. Closed System Intermittent Catheter Kit, 14 Fr (4.7mm), REF 10096140 (IPN050116).  Urinary catheter.",
      "product_quantity": "7200 catheters",
      "reason_for_recall": "Product may not be sterile",
      "recall_initiation_date": "20220920",
      "center_classification_date": "20221111",
      "report_date": "20221123",
      "code_info": "UDI (01)24026704323245(17)250405(10)74E2200810"
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