{
  "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,
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    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Medina",
      "address_1": "1065 Medina Rd Ste 500",
      "reason_for_recall": "Incorrect sizing was being laser etched on the MaxLock Extreme Mod-Foot Concave Reamer",
      "address_2": "",
      "product_quantity": "38",
      "code_info": "Part Number: MFT-074-CC-24; Lot: 3164011",
      "center_classification_date": "20141009",
      "distribution_pattern": "USA Distribution -- in the states of WI, NM, TX, WA, MO, OH, UT, TN, MI, VA, NC, VA, and PA.",
      "state": "OH",
      "product_description": "MaxLock Extreme Mod-Foot Concave Reamer; Individually packaged in a 3 x 4 bag and heat sealed with label on the outside.    Used during procedures to clear away bone and cartilage within the desired implant area.",
      "report_date": "20141015",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Orthohelix Surgical Designs Inc",
      "recall_number": "Z-0062-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69294",
      "termination_date": "20161031",
      "more_code_info": "",
      "recall_initiation_date": "20140919",
      "postal_code": "44256-5376",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}