{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Sepang",
      "state": "N/A",
      "country": "Malaysia",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79992",
      "recalling_firm": "WRP Asia Pacific Sdn Bhd",
      "address_1": "Lot 1, Perusahaan Bandar Baru",
      "address_2": "Jalan 3",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distributors in AL, CA, OH, ID, KS, MN, NC, PA, TX.",
      "recall_number": "Z-2036-2018",
      "product_description": "AmerisourceBergen PF Latex SG (Surgical Glove), Sterile, Powder Free,  Size 6.5, Item No. 10112",
      "product_quantity": "201,000 pairs",
      "reason_for_recall": "Some left-handed gloves contain powder. Powdered surgical gloves are a banned medical device in the U.S. Powder on natural rubber latex gloves can aerosolize latex allergens, resulting in sensitization to latex and allergic reactions. Additional risks of powdered gloves include severe airway inflammation, conjunctivitis, dyspnea, as well as granuloma and adhesion formation when exposed to internal tissue.",
      "recall_initiation_date": "20180507",
      "center_classification_date": "20180530",
      "termination_date": "20190530",
      "report_date": "20180606",
      "code_info": "Lot 705366565"
    }
  ]
}