{
  "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": "2026-07-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Chesapeake",
      "state": "VA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "90566",
      "recalling_firm": "Family Dollar Stores, Llc.",
      "address_1": "500 Volvo Pkwy",
      "address_2": "",
      "postal_code": "23320-1604",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Other",
      "distribution_pattern": "Nationwide within the United States",
      "recall_number": "D-1430-2022",
      "product_description": "MEDIC EYE DROPS MAX REDNESS SKU 998920   CLR EYS MX RDNS RLIF 0.5 FL OZ SKU 901844   SYSTANE ULTRA HIGH PRFRM LUB DRPS 0.14 FLOZ SKU 901961   LUMIFY REDNESS REL EYE DROPS 2.5 FL OZ\tSKU 998300   FC EYE DROPS ADVANCED 0.5 OZ SKU 902280 distributed to specific Family Dollar Stores 04/30/2022 through 06/10/2022.",
      "product_quantity": "Unknown",
      "reason_for_recall": "CGMP Deviations: product held outside appropriate storage temperature conditions.",
      "recall_initiation_date": "20220623",
      "center_classification_date": "20220822",
      "report_date": "20220831",
      "code_info": "SKUs: 998920; 901844; 901961; 998300; 902280",
      "more_code_info": ""
    }
  ]
}