{
  "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": "2026-09-09",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Wilmington",
      "state": "DE",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "99652",
      "recalling_firm": "Allies Group Inc.",
      "address_1": "1209 N Orange St",
      "address_2": "N/A",
      "postal_code": "19801-1120",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide within the U.S.A",
      "recall_number": "D-0825-2026",
      "product_description": "THE ONE SPF 50 INVISIBLE SUNSCREEN GEL, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Octisalate 5%), 20ml - 0.7 fl. oz. Tube, Made in the U.S.A, Distributed by Allies Group Pte Ltd, Singapore 068914. UPC  8 885014 074733",
      "product_quantity": "23,941, 20mL-Tube",
      "reason_for_recall": "Subpotent Product: Firm Testing indicated the affected product may not reliably provide the SPF 50 protection stated on the label.",
      "recall_initiation_date": "20260814",
      "center_classification_date": "20260831",
      "report_date": "20260909",
      "code_info": "Lots: H22V02A, Exp. 8/30/2026; C13W01B, Exp. 3/27/2027; C24W01, Exp. 4/28/2027; G23W02, Exp. 7/25/2027; G23W01B, Exp. 7/24/2027; K10W02, Exp. 10/21/2028.",
      "more_code_info": ""
    }
  ]
}