{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "56 E Bell Dr",
      "reason_for_recall": "Investigation identified that the design of the drill bit may make the suture anchor difficult to insert into the bone.  The implant may skip across the hole or miss the hole during insertion.",
      "address_2": "",
      "product_quantity": "25",
      "code_info": "Catalog:110003173, Lot 127480, 185420, 233500, 233520",
      "center_classification_date": "20131119",
      "distribution_pattern": "USA Nationwide Distribution in the states of VA, CA, Ky, and IN",
      "state": "IN",
      "product_description": "Juggerknotless Drill Bit, REF 110003173,   Sterile, Single Use    Product Usage:  The Juggerknotless Soft Anchors are indicated for soft tissue reattachment procedures in the shoulder, foot/ankle, hand/wrist, and hip.",
      "report_date": "20131127",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Biomet, Inc.",
      "recall_number": "Z-0364-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66639",
      "termination_date": "20140716",
      "more_code_info": "",
      "recall_initiation_date": "20131010",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}