FDA Medical Device Recalls (openFDA)
Shanghai United Imaging Healthcare Co., Ltd.: Positron Emission Tomography and Computed Tomography System, Model: uMI 550
- Recall number
- Z-0087-2023
- Recalling firm
- Shanghai United Imaging Healthcare Co., Ltd.
- Product
- Positron Emission Tomography and Computed Tomography System, Model: uMI 550
- Status
- Open, Classified
- Initiated
- 2022-05-30
- Posted
- 2022-10-13
- Terminated
- not on file
- Reason
- The wireless VSM module of a mobile PET/CT system, operating in an environment with strong Wi-Fi signals, may experience ECG signal and respiratory signal loss due to Wi-Fi interference. ECG and respiratory signal loss during acquisition can result in the failure of ECG and respiratory-gated reconstruction of the PET scan, which may require rescanning of the patient.
- Root cause
- Device Design
- Action
- On 5/30/22, advisory notices were emailed to customers who were asked to do the following: If the connection is not stable, perform a system reboot immediately and observe if the ECG and respiratory signals are restored. 2. If a system reboot cannot restore the wireless connection, use a third-party trigger device that supports 50ohm BNC interface and TTL output pulse with 100ms width, and connect to the system's external trigger port on the front cover. The port can be located according to Section 3.4.7 of the System Operator Manual. a) Make sure ECG and respiratory square pulse signals are displayed on the console monitor; b) Perform gated reconstruction based on the ECG and respiratory trigger pulses. 3. For further questions, please contact your recalling firm service engineer or call the Customer Contact Center's 24-hour hotline at (855) 221-1552 (toll-free) or (832) 699-2799 (direct). 4. Notify all your internal users of the PET/CT system, using this letter. 5. Complete and return the Receipt of Advisory Notification. The recalling firm will perform a design change and update the firmware of the wireless VSM module to resolve this issue. This design change is scheduled to be released for the on-site upgrade in August 2022.
- Quantity
- 32
- Distribution
- Distribution to US states of TX, WI, CA, and MI
- Lot, serial or model codes
- UDI-DI/Serial Numbers: 06971576832026/230002, 230003, 230004, 230005, 230006, 230007, 230008, 230009, 230010, 230011, 230012, 230013, 230014, 230015, 230016, 230017, 230019, 230020, 230021, 230022, 230023, 230024, 230025, 230026, 230027, 230028, 230029, 230030, 230031, 230032, 230033, 232001
- 510(k) numbers
- ["K182237","K193241"]
- PMA numbers
- not on file
- Product code
- KPS
- Firm FEI
- 3011015597
- Firm city
- Shanghai
- Firm state
- not on file
- Firm country
- China
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28