{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "West Norriton",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96615",
      "recalling_firm": "Globus Medical, Inc.",
      "address_1": "2560 General Armistead Ave",
      "address_2": "N/A",
      "postal_code": "19403-5214",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the state of AR.",
      "recall_number": "Z-1657-2025",
      "product_description": "MAGEC 2 Rod, 5.0mm 90mm Standard; Version/Model: MC2-5090S;",
      "product_quantity": "1 unit",
      "reason_for_recall": "Devices for the affected lot were not assembled  according to product specifications. The distraction rod outer diameter was assembled with a 5.5mm rod versus the required 5.0mm.",
      "recall_initiation_date": "20250403",
      "center_classification_date": "20250423",
      "report_date": "20250430",
      "code_info": "Version/Model: MC2-5090S; UDI-DI (with lot nuber):   (01)00887517834041(11)250311(17)300311(10)GB1607ET"
    }
  ]
}