{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "25434",
      "product_res_number": "Z-0653-03",
      "event_date_initiated": "2002-12-12",
      "event_date_posted": "2003-03-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-08-16",
      "res_event_number": "25233",
      "product_description": "Fetal Cell Stain Kit No. S0412-00, contents include 3 x 120ml Fetal Cell Fixing Solution (80% Reagent Alcohol), 3 x 120ml Fetal Cell Citrate Buffer Solution (Citrate Buffer, 0.081M), and 3 x 120ml Fetal Cell Stain (Erythrosin-B, Fast Green).  The responsible firm on the label is Simmler, Inc., St. Louis, MO.",
      "code_info": "Lot #92558, Exp. March, 2004",
      "firm_fei_number": "1950226",
      "recalling_firm": "Simmler Inc",
      "address_1": "4156 Hoffmeister",
      "city": "St Louis",
      "state": "MO",
      "postal_code": "63125",
      "reason_for_recall": "Fixing solution bottles are labeled as buffering solution.",
      "root_cause_description": "Other",
      "action": "Recall letters dated 12/12/02 were issued via regular mail on 12/18/02 requesting the customer to examine the contents of the kit.  If mislabeled bottles are found, they were instructed to return the kit.",
      "product_quantity": "352 kits",
      "distribution_pattern": "Distribution was made to hospitals and distributors nationwide.  Foreign distribution was made to hospitals in Canada.  Military distribution was made to hospitals in KY, OH, and Japan.",
      "openfda": {}
    }
  ]
}