{
  "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": "2026-09-02",
    "results": {
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  "results": [
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      "state": "CT",
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      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94794",
      "recalling_firm": "MICROspecialties, Inc.",
      "address_1": "430 Smith St",
      "address_2": "N/A",
      "postal_code": "06457-1531",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
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      "product_description": "Synergetics I Pack Injection Kit Custom-Tray for use with Ophthalmic injections  Model/Catalog Number: 18069  Product Description:",
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      "reason_for_recall": "Could not confirm products were exposed to the proper sterilization cycle can potentially cause post operative wound infection or injection site infection.",
      "recall_initiation_date": "20240605",
      "center_classification_date": "20240711",
      "report_date": "20240717",
      "code_info": "UDI 10841305101125 LOT: P62764965R"
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}