{
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    "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": "2026-04-01",
    "results": {
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      "city": "Morrisville",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82552",
      "recalling_firm": "Teleflex Medical",
      "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": "Nationwide",
      "recall_number": "Z-1683-2019",
      "product_description": "RUSCH LASERTUBE (Rubber), Order No. : 102004-000050, REF 102004, SIZE I.D.  mm 5,0",
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      "reason_for_recall": "The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.",
      "recall_initiation_date": "20190401",
      "center_classification_date": "20190529",
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