{
  "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-0534-2025",
      "product_description": "Medline Shoulder Repair Pack-LF, REF DYNJ82607, 2 kits/case, sterile.",
      "product_quantity": "48 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": "Lot number 24ABO552, exp. 9/30/2025, UDI-DI each 10195327198930, UDI-DI case 40195327198931.",
      "more_code_info": ""
    }
  ]
}