{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "North Haven",
      "address_1": "60 Middletown Ave",
      "reason_for_recall": "Added Instructions for Use: After application, inspect the Light Glove for barrier integrity",
      "address_2": "",
      "product_quantity": "4950 units",
      "code_info": "All lot codes in the following:    Item Number                                            Description  380789003                           SURE SET SINGLE BASIN PACK  400383006                           MAJOR BASIN PACK  400383007                           MAJOR BASIN PACK  618275004                           BASIN PACK",
      "center_classification_date": "20161108",
      "distribution_pattern": "Worldwide Distribution - US Nationwide  Foreign:  Canada:  Andorra  Austria  Belgium  Czech Republic  Denmark  Finland  France  Germany  Greece  Ireland  Israel  Italy  Latvia  Luxembourg  Monaco  Netherlands  Norway  Poland  Portugal  Russian Federation   Saudi Arabia  Slovenia  South Africa  Spain  Sweden  Switzerland  United Arab Emirates  United Kingdom",
      "state": "CT",
      "product_description": "Professional Hospital Supply, Inc Custom Packaging containing the Devon Light Glove   Item Number                                            Description  380789003                           SURE SET SINGLE BASIN PACK  400383006                           MAJOR BASIN PACK  400383007                           MAJOR BASIN PACK  618275004                           BASIN PACK    Product  Usage:  A disposable, sterile, single-use cover for compatible surgical light handles",
      "report_date": "20161116",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Covidien LLC",
      "recall_number": "Z-0366-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75302",
      "termination_date": "20190405",
      "more_code_info": "",
      "recall_initiation_date": "20160929",
      "postal_code": "06473-3908",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}