{
  "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": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Northfield",
      "address_1": "3 Lakes Dr",
      "reason_for_recall": "Product's non-conformity involves the integrity of the seal in the sterile packaging. It is possible that the seal on the sterile packaging has been compromised resulting in a loss of sterility of the medical device contained within.",
      "address_2": "",
      "product_quantity": "1031 individual packs",
      "code_info": "Item# MDS9091414A; Lots #136190",
      "center_classification_date": "20170517",
      "distribution_pattern": "Nationwide Distribution",
      "state": "IL",
      "product_description": "14 mm Distraction Pin, Exagg Qty: 1 per pack; STERILE; Manufactured for: Medline Industries, Inc., Mundelein, IL 60060 USA  Distraction Pin is designed for Anterior Cervical Fusion Procedures. Use with vertebral body distraction instruments. It is intended as a temporary fixation screw utilized during cervical spine procedures.",
      "report_date": "20170524",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "MEDLINE INDUSTRIES INC",
      "recall_number": "Z-2106-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76298",
      "termination_date": "20190709",
      "more_code_info": "",
      "recall_initiation_date": "20161214",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}