{
  "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": [
    {
      "country": "United States",
      "city": "Albany",
      "address_1": "413 N Pearl St",
      "reason_for_recall": "Possible presence of foreign material (rust).",
      "address_2": "",
      "product_quantity": "77 units Total",
      "code_info": "Lot Number: 79943  Expiration Date: March 2021",
      "center_classification_date": "20160629",
      "distribution_pattern": "Domestic - MI, MN, NJ, NM, NY & PA; International - Canada",
      "state": "NY",
      "product_description": "IMPAK ELASTIC ACRYLIC RESIN POWDER & LIQUID, SHADE TRANSPARENT, CONTENTS: 454 gm Powder + 325ml Liquid, REF 3746, Rx ONLY; Indicated for relining a denture surface",
      "report_date": "20160706",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "CMP Industries, Llc",
      "recall_number": "Z-2098-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74061",
      "termination_date": "20180525",
      "more_code_info": "",
      "recall_initiation_date": "20160428",
      "postal_code": "12207-1311",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}