{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Boston",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92481",
      "recalling_firm": "TEI Biosciences, Inc.",
      "address_1": "7 Elkins St",
      "address_2": "N/A",
      "postal_code": "02127-1601",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "recall_number": "Z-2085-2023",
      "product_description": "TissueMend; Advanced Soft Tissue Repair Matrix; Rx Only; Sizes 5x6 cm, 6x10 cm, and 3x3 cm.",
      "product_quantity": "4,832",
      "reason_for_recall": "Possible out of specification endotoxin test results due to issues with in-process and finished goods endotoxin testing.",
      "recall_initiation_date": "20230523",
      "center_classification_date": "20230703",
      "report_date": "20230712",
      "code_info": "Item No. (UDI-DI): 6495-9-001 (10381780113621), 6495-9-004 (10381780113638), 6495-9-006 (10381780113645)."
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}