{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Northfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84908",
      "recalling_firm": "Medline Industries Inc",
      "address_1": "Three Lakes Drive",
      "address_2": "N/A",
      "postal_code": "60093",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "California only. No governmental, Canadian or Mexican consignees.    TORRANCE MEMORIAL MEDICAL 3105 LOMITA BLVD TORRANCE CA 90505\u00105108     HOAG MEMORIAL HOSPITAL 1 HOAG DR NEWPORT BEACH CA 92663\u00104162     OWENS/MINOR\u0010VMI TEM (65) 5125 ONTARIO MILLS PKWY ONTARIO CA 91764\u00105103",
      "recall_number": "Z-1357-2020",
      "product_description": "Medline  HOI LUMBAR  REF DYNJ902823G  Lot 20AKA895 Expiration 2021-05-31  1 each  GTIN (01)10193489219180",
      "product_quantity": "122",
      "reason_for_recall": "The sterile pack inside the Complete Delivery System (CDS) did not go through a complete sterilization cycle, therefore the sterility of these components cannot be guaranteed.",
      "recall_initiation_date": "20200121",
      "center_classification_date": "20200225",
      "termination_date": "20230112",
      "report_date": "20200304",
      "code_info": "REF DYNJ902823G  Lot 20AKA895 Expiration 2021-05-31  1 each  GTIN (01)10193489219180"
    }
  ]
}