{
  "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": "2026-07-01",
    "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": "99062",
      "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": "US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, FL, GA, IL, KS,  KY, LA, MA, MD, MI, MN, MO, MS, MT, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, TN, TX, VA, WI,  WY and the country of Barbados.",
      "recall_number": "Z-2586-2026",
      "product_description": "Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    ANGIOGRAPHY PACK-LF\t  \tDYNJ0854485S  \t  \t  DEEP BRAIN STIMULATION PACK\t  \tDYNJ0842793G  \t\t  NEURO ACCESSORY PACK\t  \tDYNJ55385A  \t  NEURO ANGIO PACK\t  \tDYNJ51697B  \tDYNJ56509G  \tDYNJ56509I  \tDYNJ68063  \tDYNJ68845  \tDYNJ68845A  \tDYNJ68845B  \t  NEURO CERVICAL PACK\t  \tDYNJ0101287I  \tDYNJ0101287L  \t  NEURO PACK\t  \tDYNJ82103  \tDYNJ82103A  \t  NEURO TRAY\t  \tDYNJ67075  \tDYNJ67075A  \tDYNJ67075B  \t  NEURO VASCULAR PACK\t  \tDYNJ62960B  \t  NEURO VP SHUNT PACK-LF\t  \tDYNJ0843121J  \tDYNJ0843121K  \t  NEUROLOGICAL CATH PACK\t  \tDYNJ63434A  \tDYNJ63434C  \t  NEURORADIOLOGY PK\t  \tDYNJ40420D  \t  RADIOLOGY ANGIO MAJOR PACK-LF\t  \tDYNJ62858A  \t  RADIOLOGY NEURO DRAPE PAC\t  \tDYNJ61449  \t  RRMC ANGIO PACK\t  \tDYNJ36338B",
      "product_quantity": "113,843 kits",
      "reason_for_recall": "Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA.  Products not initially reported in RES 98601.",
      "recall_initiation_date": "20260227",
      "center_classification_date": "20260625",
      "report_date": "20260701",
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