{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Northfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95638",
      "recalling_firm": "MEDLINE INDUSTRIES, LP - Northfield",
      "address_1": "3 Lakes Dr",
      "address_2": "",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of AL, GA, MA, NJ, and PA.",
      "recall_number": "Z-0532-2025",
      "product_description": "(1) Medline Open Heart CDS, REF CDS840132O, packaged 1 kit/case, non-sterile; and  (2) Medline Dr. Davies CV, REF DYNJ903016G, packaged 1 kit/case, non-sterile.",
      "product_quantity": "408 kits",
      "reason_for_recall": "Some of the suture packages within the convenience kits contain the incorrect needle type/size and suture diameter/length.",
      "recall_initiation_date": "20241015",
      "center_classification_date": "20241125",
      "report_date": "20241204",
      "code_info": "(1) REF CDS840132O - Lot number 24BBF701, exp. 10/31/2024, UDI-DI each 10195327245276, UDI-DI case 40195327245277;   (2) REF DYNJ903016G - Lot numbers 24DBP801, exp. 8/31/2025; and 24CBJ749, exp. 11/30/2024, UDI-DI each - 10195327657154, UDI-DI case - 40195327657155.",
      "more_code_info": ""
    }
  ]
}