{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "status": "Terminated",
      "city": "Monroe",
      "state": "OH",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89453",
      "recalling_firm": "CellEra LLC",
      "address_1": "1045 Reed Dr Ste C",
      "address_2": "N/A",
      "postal_code": "45050-1717",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-0802-2022",
      "product_description": "20522 Vitale Silver calcium Alginate Dressings 2x2, 10/box",
      "product_quantity": "9200 ea",
      "reason_for_recall": "Firm discovered that an incorrect version of the Instructions for Use (IFU) containing language beyond the cleared 510(k) were inserted in the affected products. Firm is replacing these with the correct version of the IFU.",
      "recall_initiation_date": "20211215",
      "center_classification_date": "20220316",
      "termination_date": "20231016",
      "report_date": "20220323",
      "code_info": "Lot 229999 GTIN 10856276008762, 00856276008765, 00856276008758"
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}