{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Horby",
      "state": "",
      "country": "Sweden",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87635",
      "recalling_firm": "Atos Medical AB",
      "address_1": "Kraftgatan 8",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide distribution in the states of IL, CT, VA, NM, NY, SC, NJ, OK, MN, MI, NC, OH, AZ, WI, CA, PA, ID.",
      "recall_number": "Z-1548-2021",
      "product_description": "Provox Life Night HME, Catalogue Number 8262 - Product Usage:  single use heat and moisture exchangers for patients breathing through a tracheostoma.",
      "product_quantity": "225 boxes of 30 devices",
      "reason_for_recall": "Provox Life Night HME may be incorrectly inserted sideways or forcefully through the adhesive coupling potentially occluding or blocking the stoma.",
      "recall_initiation_date": "20210329",
      "center_classification_date": "20210510",
      "termination_date": "20220217",
      "report_date": "20210519",
      "code_info": "Lot Numbers:  2012158 and 2012124",
      "more_code_info": ""
    }
  ]
}