{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Grand Rapids",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90834",
      "recalling_firm": "SunMed Holdings, LLC",
      "address_1": "2710 Northridge Dr Nw Ste A",
      "address_2": "N/A",
      "postal_code": "49544-9112",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Domestic distribution to AL, FL, GA, IL, LA, MO, NJ, NY, TN, TX.",
      "recall_number": "Z-1779-2022",
      "product_description": "Full Kit Pulset 3cc Syringe 23g x 1  Safety Tip 25u BH,  REF Number 3373-91",
      "product_quantity": "53,560 units",
      "reason_for_recall": "The kits are being recalled due to a lack of sterility of a spare needle contained within the kits. There is a potential for skin infection or sepsis if the patient is exposed to a non-sterilized, unused needle.",
      "recall_initiation_date": "20220908",
      "center_classification_date": "20220923",
      "termination_date": "20240618",
      "report_date": "20221005",
      "code_info": "UDI-DI: 00709078004483 (each label); 10709078004480 (box label)  Lots 010822N23, 052521N54, 081821N05, 101221N11"
    }
  ]
}