{
  "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
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  },
  "results": [
    {
      "country": "United States",
      "city": "Zelienople",
      "address_1": "Jackson Pointe Commerce",
      "reason_for_recall": "The surgical gowns were manufactured in a facility that is not registered by the FDA.",
      "address_2": "4050 Jacksons Pointe Ct",
      "product_quantity": "2, 868 total kits",
      "code_info": "WPGA21L; Lot # 998201, Exp. Date 01/02/2021 (24 kits) and Lot # 6781914, Exp date 11/18/2020 (4 kits)  AGGL48H; Lot# 643191, Exp. Date 12/23/2020 (80 kits)  AGGM59N: Lot # 761191, Exp. Date 08/27/2020 (5 kits)",
      "center_classification_date": "20200529",
      "distribution_pattern": "US Nationwide distribution including in the state of Pennsylvania.",
      "state": "PA",
      "product_description": "Custom Packs to be used in surgical procedures.",
      "report_date": "20200610",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "American Contract Systems",
      "recall_number": "Z-2168-2020",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "85502",
      "termination_date": "20201125",
      "recall_initiation_date": "20200413",
      "postal_code": "16063-2838",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}