{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "El Segundo",
      "state": "CA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85388",
      "recalling_firm": "Karl Storz Endoscopy",
      "address_1": "2151 E Grand Ave",
      "address_2": "N/A",
      "postal_code": "90245-5017",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "57 consignees in the US. AL,AZ,CA,CT,DE,FL,GA,IL,LA,MA,MD,ME,MI,MN,NE,NH,NJ,NY,OH,OK,PA,SC,TX,VA,VT,WA and WI",
      "recall_number": "Z-1942-2020",
      "product_description": "Insufflation tubing to be used with varies insufflator units. REF 031200-10; REF 031322-10; REF 031532-10; REF 031622-10",
      "product_quantity": "543 boxes were distributed; 10 ea per box.",
      "reason_for_recall": "The sterile single-use tubing may contain higher ethylene oxide (EO) residues than the acceptable level.",
      "recall_initiation_date": "20190109",
      "center_classification_date": "20200508",
      "termination_date": "20220928",
      "report_date": "20200520",
      "code_info": "Model/Lot Number:     031200-10/Lot W-027781, W-029058, W-028738;  031322-10/ Lot W-027197, W-028171, W-027939, W-028207;  031532-10/ Lot W-026437, W-027332, W-026871;  031622-10/Lot W-029555"
    }
  ]
}