{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
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  "results": [
    {
      "cfres_id": "101903",
      "product_res_number": "Z-0446-2012",
      "event_date_initiated": "2011-04-27",
      "event_date_posted": "2012-01-11",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-06-06",
      "res_event_number": "59231",
      "product_code": "GXP",
      "k_numbers": [
        "K051093"
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      "product_description": "Osteopore PCL Scaffold Bone Filler: Osteopore Osteoplug-C, Osteoplug, and Osteomesh.",
      "code_info": "Serial number LP-07-000695-714, lot number P0009032007-NW-05, expiry date Jul-12;  Serial number TT-07-002201-2500, lot number P0009032007-NW-05, expiry date Sep-12; and Serial number PL-09-000006 to 15, lot number P0010112007-NW-05, expiry date Dec-12.",
      "firm_fei_number": "3007303685",
      "recalling_firm": "OSTEOPORE INTERNATIONAL PTE LTD",
      "address_1": "10, SCIENCE PARK ROAD 10 SCIENCE PARK ROAD THE ALPHA #02-28",
      "city": "SINGAPORE",
      "country": "SINGAPORE",
      "reason_for_recall": "Product sterility may be compromised.",
      "root_cause_description": "Nonconforming Material/Component",
      "action": "Osteopore sent an Urgent Voluntary Product Recall notice to  their consignees by letter dated April 27, 2011.",
      "product_quantity": "330",
      "distribution_pattern": "Nationwide distribution - one distributor in TX.",
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        "device_name": "Methyl Methacrylate For Cranioplasty",
        "medical_specialty_description": "Neurology",
        "regulation_number": "882.5300",
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