{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Deerfield",
      "address_1": "1 Baxter Pkwy",
      "reason_for_recall": "Potential presence of rust on Coupler Forceps (GEM4183C).",
      "address_2": "",
      "product_quantity": "123 devices",
      "code_info": "Product Code 5193-06001-010, Lot Number: SP18E129-1307852, Sub-lot Number: 90828, UDI: 00844735002850",
      "center_classification_date": "20181222",
      "distribution_pattern": "Nationwide distribution to CA, FL, GA, KS, LA, MA, MS, NE, NJ, NV, NY, OH, PA, TX, UT, VA, WA, WV.      International distribution to United Kingdom, Germany, South Africa, Japan, and  Australia",
      "state": "IL",
      "product_description": "GEM Coupler Forceps, GEM4183C, packaged individually.",
      "report_date": "20190102",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Baxter Healthcare Corporation",
      "recall_number": "Z-0680-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "81581",
      "more_code_info": "",
      "recall_initiation_date": "20181102",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}