{
  "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-0533-2025",
      "product_description": "(1) Medline Pacer Implant Pack, REF DYNJ59194A, 4 kits/case, sterile; and  (2) Medline Thoracotomy Morristown, REF DYNJ904220F, 1 kit/case, non-sterile.",
      "product_quantity": "360 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 DYNJ59194A - Lot numbers 24DLA916, exp. 12/31/2025; and 24BLA030, exp. 11/30/2025; UDI-DI each 10193489573480, UDI-DI case 40193489573481; and  (2) REF DYNJ904220F - Lot number 24DLA070, exp. 11/30/2024, UDI-DI each 10195327362300, UDI-DI case 40195327362301.",
      "more_code_info": ""
    }
  ]
}