{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Abingdon",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65286",
      "recalling_firm": "Penlon, Ltd.",
      "address_1": "Abingdon Science Park",
      "address_2": "Barton Lane",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA including FL, KY, PA, ND, MN, IL, NJ, TX, TN, and VA.   Internationally to Belgium, China, Czech Republic, France, Germany, Switzerland, Australia, Finland, Holland, Lithunia, Malta, Poland, and Slovakia.",
      "recall_number": "Z-1653-2013",
      "product_description": "Delta Vaporizer    An anesthetic vaporizer is a device used to vaporize liquid anesthetic and deliver a controlled amount of the vapor to the patient.",
      "product_quantity": "9208 (of which 576 were within the US)",
      "reason_for_recall": "It has come to Penlon Ltd's attention of an instance where the installation and pre-use checks listed in the User Manual may not have been followed prior to the clinical use of the vaporizer.  Penlon Ltd has updated the Installation and daily Pre-Use Check sections of the User Manual to ensure that the instructions are explicit and clear.",
      "recall_initiation_date": "20130514",
      "center_classification_date": "20130702",
      "termination_date": "20140512",
      "report_date": "20130710",
      "code_info": "All; recalled products are traced by serial numbers D0312-XXXX to D1112-XXXX."
    }
  ]
}