{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "Parsippany",
      "address_1": "10 Pomeroy Rd",
      "reason_for_recall": "Zimmer Biomet is initiating a recall of specific lots of foil pouched, sterile Trabecular Metal implants that were manufactured between April 2011 and October 2012. The foil pouches are part of a dual barrier system to provide sterile integrity.",
      "address_2": "",
      "product_quantity": "19,884 total",
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      "center_classification_date": "20160610",
      "distribution_pattern": "Nationwide and Foreign.",
      "state": "NJ",
      "product_description": "POROUS PATELLA 32MM X 10MM - 00587806532    POROUS PATELLA 35MM X 10MM-  00587806535    POROUS PATELLA 38MM X 10MM - 00587806538    POROUS PATELLA 41MM X 10MM - 00587806541",
      "report_date": "20160622",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Trabecular Metal Technology, Inc.",
      "recall_number": "Z-1950-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "73536",
      "termination_date": "20171129",
      "more_code_info": "",
      "recall_initiation_date": "20160415",
      "postal_code": "07054-3722",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}