{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "26857",
      "product_res_number": "Z-0864-03",
      "event_date_initiated": "2003-03-31",
      "event_date_posted": "2003-05-22",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-09-22",
      "res_event_number": "26006",
      "product_code": "MAA",
      "k_numbers": [
        "K884632"
      ],
      "product_description": "Acuson Diagnostic Ultrasound System Transducer;\nModel Number(s):  L582 Linear Array Transducer for use on the 128XP Ultrasound System;\nCatalog Numbers:  23656 (New), 45441 (Refurb)",
      "code_info": "All Serial Numbers: XXXXXXXX (8-digit)",
      "firm_fei_number": "2936884",
      "recalling_firm": "Siemens Medical Solutions USA, Inc.",
      "address_1": "1230 Shorebire Way",
      "address_2": "P.O. Box 7393",
      "city": "Mountain View",
      "state": "CA",
      "postal_code": "94039-7393",
      "reason_for_recall": "The product has a software condition in that the surface temperature of the transducer may reach above the thermal limit.",
      "root_cause_description": "Other",
      "action": "On 3/24/03, the firm issued letters via US Mail to all its direct consignees informing them of the affected device and providing instructions on the recall.",
      "product_quantity": "220 units",
      "distribution_pattern": "Nationwide and worldwide. The product received nationwide distribution to 123 consignees: 23 Distributors (50 transducers) and consumers/users: approximately 100 customers (146 transducers).  2 transducers were consigned to Federal Government locations: (1) Martin Army Community Hospital, 9200 Marne Rd., Fort Benning, GA 31905, (2) Lackland AFB, Wilford Hall, 2200 Bergquist Dr., #100, Lackland AFB, TX 78236.  The firm has also distributed product into international channels through distributors.  Countries include, Austria; Barbados; Brazil; Canada; China (PRC); Egypt, France, Germany; Greece; India; Italy; Japan; South Korea; Netherlands; Russia; Saudi Arabia; Sweden; Taiwan; and United Kingdom.  There is no Canadian distribution.  The firm is continuing to obtain the international distribution through the distributors.  The recall was appropriately extended to the consumer/user level; i.e., the wholesalers/distributors, and users who received the recalled product.",
      "openfda": {
        "k_number": [
          "K102138",
          "K895909",
          "K905456",
          "K915138",
          "K905536",
          "K894992",
          "K090499",
          "K904600",
          "K904951"
        ],
        "registration_number": [
          "1216677"
        ],
        "fei_number": [
          "1216677"
        ],
        "device_name": "Monitor, Fetal Doppler Ultrasound",
        "medical_specialty_description": "Obstetrics/Gynecology",
        "regulation_number": "884.2660",
        "device_class": "2"
      }
    }
  ]
}