{
  "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": [
    {
      "status": "Terminated",
      "city": "Cirencester",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88589",
      "recalling_firm": "Corin Ltd",
      "address_1": "Unit 1-57-8",
      "address_2": "Corinium Centre",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of AZ, CA, FL, IL, OK, PA, TX, UT, and WI.",
      "recall_number": "Z-2610-2021",
      "product_description": "Corin Unity Knee Augments, Size 5, 6 & 7 / 10mm Thick, Femoral Posterior Augment, REF 1122370, Sterile, a component of the Unity Total Knee System.",
      "product_quantity": "1 unit",
      "reason_for_recall": "The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices.",
      "recall_initiation_date": "20210728",
      "center_classification_date": "20210930",
      "termination_date": "20240612",
      "report_date": "20211006",
      "code_info": "The affected products are shipment specific and were delivered to the consignee between 7/22-26/2021.   Lot number 472687 was delivered 7/23/2021."
    }
  ]
}