{
  "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": "Minneapolis",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85375",
      "recalling_firm": "Smiths Medical ASD Inc.",
      "address_1": "6000 Nathan Ln N",
      "address_2": "N/A",
      "postal_code": "55442-1690",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of MA, MD, MO and IN.",
      "recall_number": "Z-1820-2020",
      "product_description": "Portex Lumbar Puncture Tray. Anesthesia Conduction Kit. 4826PL-20 - Product Usage: Portex lumbar puncture trays provide all the materials necessary to measure cerebrospinal fluid pressure and/or collect cerebrospinal fluid specimens. Key components include skin prep materials, lancet-point needle, manometer with stopcock and extension set, and specimen vials.",
      "product_quantity": "100 units.",
      "reason_for_recall": "Cases of Portex¿ Lumbar Puncture Tray Child, SKU #4826PL-20 had been mislabeled with  invalid information. The product was correct, but the inner trays were labeled as 4824PL-20 instead of 4826PL-20.",
      "recall_initiation_date": "20200228",
      "center_classification_date": "20200429",
      "termination_date": "20210901",
      "report_date": "20200506",
      "code_info": "Lot #3842192, Model no. 4826PL-20."
    }
  ]
}