{
  "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": "2026-09-12",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "194859",
      "product_res_number": "Z-1514-2022",
      "event_date_initiated": "2022-07-07",
      "event_date_created": "2022-08-11",
      "recall_status": "Open, Classified",
      "res_event_number": "90585",
      "product_code": "FEO",
      "k_numbers": [
        "K171024"
      ],
      "product_description": "ShockPulse-SE Lithotripsy Generator\nModel/Serial: SPL-S",
      "code_info": "UDI-DI: 00821925044197\nSerial numbers: CG5085 and CG6009",
      "firm_fei_number": "2429304",
      "recalling_firm": "Olympus Corporation of the Americas",
      "address_1": "3500 Corporate Pkwy",
      "city": "Center Valley",
      "state": "PA",
      "postal_code": "18034-8229",
      "additional_info_contact": "SAME\n484-896-5000",
      "reason_for_recall": "Mis-wired component-the improperly wired component can result in additional noise on the power supply output. Noise on the ultrasonic input circuit is not consistent with electromagnetic compatibility (EMC) standards and may decrease the overall reliability of the system and result in delay of treatment",
      "root_cause_description": "Process change control",
      "action": "Olympus issued Urgent Medical Device Recall Letter dated July 7, 2022. Letter states reason for recall, health risk and action to take:\n1. Immediately locate the generator with the serial numbers listed in this communication. The serial number is located on the back of the unit.\n2. Your sales representative will work with you to arrange for the return of your unit and assist with initiating an order for a replacement unit.\n3. Olympus requests that you acknowledge receipt of this letter by accessing the Olympus recall portal. Go to https://olympusamerica.com/recall. Enter the recall number  0410  and provide your contact information as indicated in the portal.\n4. If you have distributed these devices outside your facility, please notify your customers of this removal action immediately. Your notification to your customers may be enhanced by including a copy of this recall notification letter.\n\nContact (647) 999-3203 or at Cynthia.Ow@Olympus.com for any additional information or support concerning this matter.",
      "product_quantity": "2 units",
      "distribution_pattern": "US Nationwide distribution in the states of AL, NM.",
      "openfda": {
        "k_number": [
          "K181997",
          "K142428",
          "K171024",
          "K181364",
          "K173234",
          "K850298",
          "K920235",
          "K993046",
          "K973251",
          "K182490",
          "K843101",
          "K842024",
          "K230893",
          "K873367"
        ],
        "registration_number": [
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          "3006617533",
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          "3010707607",
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        "fei_number": [
          "3004096429",
          "3007475226",
          "1000136269",
          "3006617533",
          "3010707607",
          "3014342096",
          "3003790304",
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          "3024021261",
          "2020550",
          "1220477",
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          "3011050570",
          "2528981",
          "3002806910",
          "2183744",
          "3002808268",
          "2435119",
          "3002808001"
        ],
        "device_name": "Lithotriptor, Ultrasonic",
        "medical_specialty_description": "Gastroenterology, Urology",
        "regulation_number": "876.4480",
        "device_class": "2"
      }
    }
  ]
}