{
  "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": "2026-06-24",
    "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": "98601",
      "recalling_firm": "Medline Industries, LP",
      "address_1": "3 Lakes Dr",
      "address_2": "N/A",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Canada, Panama, Barbados.",
      "recall_number": "Z-1889-2026",
      "product_description": "Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes    E P DRAPE PACK-LF\tDYNJ0373061J",
      "product_quantity": "270,311 total",
      "reason_for_recall": "Unapproved design changes to the products outside of the 510(k) clearance.",
      "recall_initiation_date": "20260227",
      "center_classification_date": "20260417",
      "report_date": "20260429",
      "code_info": "DYNJ0373061J  UDI-DI 10889942396856 (EA) 40889942396857 (CS) LOT  24ABR895",
      "more_code_info": ""
    }
  ]
}