{
  "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": "Completed",
      "city": "Manchester",
      "state": "NH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92131",
      "recalling_firm": "IMMUNDIAGNOSTIK, Inc",
      "address_1": "400 Bedford St Ste 104",
      "address_2": "N/A",
      "postal_code": "03101-1195",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide Distribution: CA, IL, NC, NH, OR",
      "recall_number": "Z-1603-2023",
      "product_description": "Immundiagnostik IDK Lactoferrin ELISA- In vitro enzyme immunoassay intended for the determination of lactoferrin in stool. P/N: K6870   Single Kit P/N: K6870.20.US.L   20 Plates",
      "product_quantity": "88 units",
      "reason_for_recall": "Marketed without a 510k",
      "recall_initiation_date": "20230327",
      "center_classification_date": "20230517",
      "report_date": "20230524",
      "code_info": "UDI: (01) 04050598000582 PN K6870/Lot Numbers:  220706 Exp. 05/04/2024;  221122 Exp. 06/07/2024.  P/N:K6870.20.US.L Lot Numbers:  221124 Exp:07/29/2025, 230102 Exp: 10/24/2025"
    }
  ]
}