{
  "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-1424-2022",
      "product_description": "FW ASPIRIN CHEWABLE TABLET 36CT SKU 913990  GS ENTERIC ASPIRIN TABLET 120 CT SKU 913724   BAYER BACK BODY EX STRGTH CAPLETS 24CT SKU 900438   BAYER LOW DOSE 81 MG TABLET 120 CT SKU 916070   BAYER ASPIRIN 325MG TABLET 24CT SKU 913996   BAYER LOW DOSE TABLET 32CT SKU 915641   BAYER 81MG CHEWABLE TABLET 36 CT SKU 916078 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: 913990; 913724; 900438; 916070; 913996; 915641; 916078",
      "more_code_info": ""
    }
  ]
}