{
  "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": "96374",
      "recalling_firm": "MEDLINE INDUSTRIES, LP - Northfield",
      "address_1": "3 Lakes Dr",
      "address_2": "N/A",
      "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 country of Canada.",
      "recall_number": "Z-1436-2025",
      "product_description": "Medline procedure kits labeled as:    1) ANGIO PACK, Pack Number DYNJ50624A;   2) ANGIO PACK, Pack Number DYNJ30501F;   3) ANGIO PACK-LF, Pack Number DYNJ0954970G;   4) ANGIOGRAPHY 6 FRENCH PACK, Pack Number DYNJ33597J;   5) ANGIOGRAPHY DRAPE PACK, Pack Number DYNJ38120B;   6) ANGIOGRAPHY DRAPE PACK, Pack Number DYNJ42873;   7) ANGIOGRAPHY PACK, Pack Number DYNJ57498;   8) ANGIOGRAPHY PACK, Pack Number DYNJ52167A;   9) ANGIOGRAPHY PACK, Pack Number DYNJV0173I;   10) ANGIOGRAPHY TRAY-LF, Pack Number DYNJ58722A;   11) CATH LAB PACK, Pack Number DYNJ42912F;   12) CATH LAB PK, Pack Number DYNJ35643B;   13) CATH PACK-LF, Pack Number DYNJ0367643Q;   14) CRMS ANGIO PACK-LF, Pack Number PHS616026002A;   15) DEPAUL ANGIO CATH PACK, Pack Number DYNJ24542L",
      "product_quantity": "1939 units",
      "reason_for_recall": "Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.",
      "recall_initiation_date": "20250211",
      "center_classification_date": "20250325",
      "report_date": "20250402",
      "code_info": "1) Pack Number DYNJ50624A:   UDI/DI 10889942474639 (each) 40889942474630 (case), Lot Number 20BDB393A;  2) Pack Number DYNJ30501F:   UDI/DI 10889942806683 (each) 40889942806684 (case), Lot Number 21HBP134A;  3) Pack Number DYNJ0954970G:   UDI/DI 10193489505634 (each) 40193489505635 (case), Lot Number 21GMA850A;  4) Pack Number DYNJ33597J:   UDI/DI 10889942802012 (each) 40889942802013 (case), Lot Number 21IMD296A;  5) Pack Number DYNJ38120B:   UDI/DI 10884389722145 (each) 40884389722146 (case), Lot Number 21BBI114A;  6) Pack Number DYNJ42873:   UDI/DI 10888277011298 (each) 40888277011299 (case), Lot Number 23EBE560A;  7) Pack Number DYNJ57498:   UDI/DI 10889942745746 (each) 40889942745747 (case), Lot Number 21AMA569A;  8) Pack Number DYNJ52167A:   UDI/DI 10193489541106 (each) 40193489541107 (case), Lot Number 21GMB606A;  9) Pack Number DYNJV0173I:   UDI/DI 10889942965021 (each) 40889942965022 (case), Lot Number 23CLA070A;  10) Pack Number DYNJ58722A:   UDI/DI 10193489329698 (each) 40193489329699 (case), Lot Number 21IME955A;  11) Pack Number DYNJ42912F:   UDI/DI 10193489785753 (each) 40193489785754 (case), Lot Number 23LBU921Z;  12) Pack Number DYNJ35643B:   UDI/DI 10193489223712 (each) 40193489223713 (case), Lot Number 21BBG490A;  13) Pack Number DYNJ0367643Q:   UDI/DI 10193489648614 (each) 40193489648615 (case), Lot Number 23EBE428A;  14) Pack Number PHS616026002A:   UDI/DI 10889942429370 (each) 40889942429371 (case), Lot Number 23BBS889A;  15) Pack Number DYNJ24542L:   UDI/DI 10193489651119 (each) 40193489651110 (case), Lot Number 20FBN798A"
    }
  ]
}