{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Medley",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91723",
      "recalling_firm": "Entopsis , Inc.",
      "address_1": "7600 Nw 69th Ave",
      "address_2": "N/A",
      "postal_code": "33166-2521",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide and  Canada, UK, Portugal, England, Spain, England , Germany, Brazil, Denmark, KOR, South Korea, Colombia, Lithuania",
      "recall_number": "Z-1297-2023",
      "product_description": "PCRopsis Activator: a)  1.5mL, REF 228001; b) 0.5mL,REF 228002; nucleic acid extraction from a variety of biological samples",
      "product_quantity": "52 units",
      "reason_for_recall": "Presence of misleading label statements on the product label.",
      "recall_initiation_date": "20230221",
      "center_classification_date": "20230329",
      "report_date": "20230405",
      "code_info": "a) REF 282001: Lot Numbers:  3, Exp. 05/2023; 4, Exp. 07/2023; b) REF 228002: Lot Numbers:  3, Exp. 05/2023; 4, Exp. 07/2023; 5, Exp. 04/2023"
    }
  ]
}