{
  "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",
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      "recalling_firm": "TEI Biosciences, Inc.",
      "address_1": "7 Elkins St",
      "address_2": "N/A",
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      "voluntary_mandated": "Voluntary: Firm initiated",
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      "product_description": "SurgiMend PRS Meshed; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Size 10cm x 20cm",
      "product_quantity": "9,215 units",
      "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. 606-907-001. No UDI-DI (Distributed in Canada and EU)."
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}