{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
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  "results": [
    {
      "status": "Ongoing",
      "city": "Noblesville",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95451",
      "recalling_firm": "King Systems Corp. dba Ambu, Inc.",
      "address_1": "15011 Herriman Blvd",
      "address_2": "N/A",
      "postal_code": "46060-4253",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide",
      "recall_number": "Z-0270-2025",
      "product_description": "KING LTSD,SIZE 1,W/SUCTION PORT STERILE-Inserted into a patient s pharynx through the mouth to provide  patent airway.  Model/Catalog Number: KLTSD421",
      "product_quantity": "21939 units",
      "reason_for_recall": "Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because it introduces a new indication for pediatric use in an Oropharyngeal Airway.",
      "recall_initiation_date": "20240926",
      "center_classification_date": "20241030",
      "report_date": "20241106",
      "code_info": "UDI-DI: 00612649210162 (Shipper Label); 00612649210155 (Piece Label)",
      "more_code_info": ""
    }
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}