{
  "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-2595-2026",
      "product_description": "Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    PICC LINEPACK (PCLUI)642-LF\t  \tDYNJ47717A",
      "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",
      "code_info": "DYNJ47717A    UDI-DI 10193489454529    Lots 21CMD153   21EMC033   21HMB521   21HMF278   21IME100   21IMG896   21JMG286   22AME235   22BMH056   22EMF125   22GMI215   22JME782   22LMC139   22LMC336"
    }
  ]
}