{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Wappingers Falls",
      "address_1": "PO Box 1840",
      "reason_for_recall": "The On/Off functionality in the LCSU 4 is controlled by electronic components, one of which might be damaged.",
      "address_2": "167 Myers Corners Rd",
      "product_quantity": "4,377 units",
      "code_info": "Affected units are labelled with Manufacturing Dates in the range 20150501 to 20161028.",
      "center_classification_date": "20170420",
      "distribution_pattern": "Nationwide",
      "state": "NY",
      "product_description": "Laerdal Compact Suction Unit ¿ 4 under the following labels: 1) 300 ml (3.3 lbs) canister version - CATALOG #(s): 88006101 - LCSU 4, 300 ml Complete unit (US), 88006103 - LCSU 4, 300 ml Complete unit (UK), 88006140 - LCSU 4, 300 ml Complete unit (EUR), 881151 - Replacement unit, 88006201 - LCSU 4, 300 ml, RTCA Complete unit (US), 88006203 - LCSU 4, 300 ml, RTCA Complete unit (UK), 88006240 - LCSU 4, 300 ml, RTCA Complete unit (EUR) and 881152 - Replacement Unit, RTCA; 2)  88005101 - LCSU 4, 800 ml Complete unit (US), 88005103 - LCSU 4, 800 ml Complete unit (UK), ¿ 88005140 - LCSU 4, 800 ml Complete unit (EUR), 88005201 - LCSU 4, 800 ml, RTCA Complete unit (US), 88005203 - LCSU 4, 800 ml, RTCA Complete unit (UK), 88005240 - LCSU 4, 800 ml, RTCA Complete unit (EUR)                & 2) 800 ml (4.3 lbs) canister version - CATALOG #(s): 88005101, 88005201 (RTCA)",
      "report_date": "20170426",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Laerdal Medical Corporation",
      "recall_number": "Z-1873-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76744",
      "termination_date": "20180525",
      "recall_initiation_date": "20170108",
      "postal_code": "12590-3869",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}