{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Northfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92204",
      "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": "Letter",
      "distribution_pattern": "Distribution was made to California.  There was no foreign/government/military distribution.",
      "recall_number": "Z-1646-2023",
      "product_description": "Procedure packs:    (1) Medline Sterile Arthroscopy Pack, REF: DYNJ64242B;  (2) Medline Sterile Shoulder Pack, REF: DYNJ64250A; and  (3) Medline Sterile Upper Extremity Pack, REF: DYNJ64253B.",
      "product_quantity": "342 packs (114 packs/product)",
      "reason_for_recall": "The kits were damaged by water.",
      "recall_initiation_date": "20230421",
      "center_classification_date": "20230526",
      "report_date": "20230607",
      "code_info": "(1) Arthroscopy Pack - Lot #22HMD098, Exp. 2024-04-30, UDI/DI (01)10193489956405; (2) Shoulder Pack -Lot #22JMA673, Exp. 2024-01-31, GTIN (01)10193489429817; and (3) Upper Extremity Pack - Lot #HMF900, Exp. 2024-01-31, UDI/DI (01)10193489968453."
    }
  ]
}