{
  "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": "98994",
      "recalling_firm": "Medline Industries, LP",
      "address_1": "3 Lakes Dr",
      "address_2": "",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of AE, BB, BM, BS, CA, CY, GU, NL, PA, QA, SA, VI.",
      "recall_number": "Z-2500-2026",
      "product_description": "MEDLINE Medical Procedure Kits labeled as:    1) CAROTID NEURO PACK, Medline Kit Number/SKU DYNJ44926G;   2) VP SHUNT CDS, Medline Kit Number/SKU CDS983800J;   3) VP SHUNT CDS, Medline Kit Number/SKU CDS983800K.",
      "product_quantity": "342 units",
      "reason_for_recall": "During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.",
      "recall_initiation_date": "20260504",
      "center_classification_date": "20260617",
      "report_date": "20260624",
      "code_info": "Medline Kit Number/SKU  DYNJ44926G:  UDI/DI 10193489766554 (each), 40193489766555 (case), Lot Number 24EBH848;  Medline Kit Number/SKU  DYNJ44926G:  UDI/DI 10193489766554 (each), 40193489766555 (case), Lot Number 24DBK995;  Medline Kit Number/SKU  DYNJ44926G:  UDI/DI 10193489766554 (each), 40193489766555 (case), Lot Number 23JBP023;  Medline Kit Number/SKU  DYNJ44926G:  UDI/DI 10193489766554 (each), 40193489766555 (case), Lot Number 23HBR067;  Medline Kit Number/SKU  DYNJ44926G:  UDI/DI 10193489766554 (each), 40193489766555 (case), Lot Number 23FBM330;  Medline Kit Number/SKU  DYNJ44926G:  UDI/DI 10193489766554 (each), 40193489766555 (case), Lot Number 23EBK061;  Medline Kit Number/SKU  DYNJ44926G:  UDI/DI 10193489766554 (each), 40193489766555 (case), Lot Number 22JBG042;  Medline Kit Number/SKU  DYNJ44926G:  UDI/DI 10193489766554 (each), 40193489766555 (case), Lot Number 22GBH864;  Medline Kit Number/SKU  DYNJ44926G:  UDI/DI 10193489766554 (each), 40193489766555 (case), Lot Number 22DBT571;  Medline Kit Number/SKU  CDS983800J:  UDI/DI 10195327684662 (each), 40195327684663 (case), Lot Number 25DMJ438;  Medline Kit Number/SKU  CDS983800J:  UDI/DI 10195327684662 (each), 40195327684663 (case), Lot Number 25CMH178;  Medline Kit Number/SKU  CDS983800J:  UDI/DI 10195327684662 (each), 40195327684663 (case), Lot Number 24IME720;  Medline Kit Number/SKU  CDS983800J:  UDI/DI 10195327684662 (each), 40195327684663 (case), Lot Number 24HMG912;  Medline Kit Number/SKU  CDS983800K:  UDI/DI 10198459518973 (each), 40198459518974 (case), Lot Number 26CMC503;  Medline Kit Number/SKU  CDS983800K:  UDI/DI 10198459518973 (each), 40198459518974 (case), Lot Number 26AMB047;  Medline Kit Number/SKU  CDS983800K:  UDI/DI 10198459518973 (each), 40198459518974 (case), Lot Number 25JME109.",
      "more_code_info": ""
    }
  ]
}