{
  "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": "Ongoing",
      "city": "Saint Paul",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90989",
      "recalling_firm": "3M Healthcare Business",
      "address_1": "2510 Conway Ave E",
      "address_2": "N/A",
      "postal_code": "55144-4147",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide distribution.",
      "recall_number": "Z-0256-2023",
      "product_description": "3M Steri-Drape, Small Drape with Incise Film, REF 1021NS, general surgery drape",
      "product_quantity": "104,000 units",
      "reason_for_recall": "During a recent investigation, 3M confirmed the liner on the adhesive component of the affected drapes is difficult to remove without damaging the product and may render the product unusable. Additionally, 3M has observed an increase in reported adhesive related skin injuries for these affected lots.",
      "recall_initiation_date": "20221006",
      "center_classification_date": "20221118",
      "report_date": "20221130",
      "code_info": "UDI/DI (01)50707387497410, Lot numbers:  33HT9W, 33HWN8, 33J5T9, 33JL66, 33JLLW, 33JMKR, 33JN4N, 33K7Y7, 33K888"
    }
  ]
}