{
  "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
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Trumbull",
      "address_1": "95 Corporate Dr",
      "reason_for_recall": "Mislabeled: Printing on the top web or Tyvek lid  of the individual product blister tray indicating that it contains a Pipet Current or Part Number MX140 and the display box indicating the correct Os FinderTM Cervical Dilators, Part Number 1176. The product in the individual product package is the correct Os Finder Cervical Dilator",
      "address_2": "",
      "product_quantity": "2,250 units (45 boxes of 50)",
      "code_info": "Lot 284288 - Expiration date: 02/24/2023",
      "center_classification_date": "20200704",
      "distribution_pattern": "Nationwide",
      "state": "CT",
      "product_description": "COOPERSURGICAL Os FinderTM Cervical Dilator,   Taper: 2.0 mm to 4.0 mm OD Length: 21.5 cm  Box of 50  Part Number: 1176",
      "report_date": "20200715",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "CooperSurgical, Inc.",
      "recall_number": "Z-2498-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "85787",
      "termination_date": "20210511",
      "more_code_info": "",
      "recall_initiation_date": "20200603",
      "postal_code": "06611-1350",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}