{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Burlington",
      "address_1": "154 Middlesex Tpke",
      "reason_for_recall": "A locking plastic abutment sleeve, used by dental technicians in dental laboratories to aid in the creation of the final restorative crown, was packed as a non-locking plastic abutment sleeve.",
      "address_2": "",
      "product_quantity": "55",
      "code_info": "Lots: 35026, 35579, 36133",
      "center_classification_date": "20180324",
      "distribution_pattern": "International Distribution to: Germany only.",
      "state": "MA",
      "product_description": "STAGE-1¿ RDS COC Abutment Plastic Sleeve, Non-Lock, Multi-Unit; Catalog Number: S2437-01-1K",
      "report_date": "20180404",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Keystone Dental Inc",
      "recall_number": "Z-1179-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "79297",
      "termination_date": "20190417",
      "more_code_info": "",
      "recall_initiation_date": "20171016",
      "postal_code": "01803-4403",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}