SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION: Device Recall
Recall #Z-0139-2025 · 09/06/2024
Class II: Risk
Recall Details
- Recall Number
- Z-0139-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION
- Status
- Ongoing
- Date Initiated
- 09/06/2024
- Location
- Kyoto, N/A, Japan
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 13
Reason for Recall
If digital angiography system is used with a specific catheterization table and the operator directs simultaneous movement of the table and the C-arm using direct memory, then direct memory button is released, the table may continue to move, which the operator can stop by pressing the stop button.
Product Description
Trinias unity, Digital Angiography System with Catheterization Table, Model: KS-100 This system consists of the following main components: C arm, catherization table, image processing equipment, x-ray high voltage generator, x-ray tube. There are several types of each component.
Distribution Pattern
US Nationwide distribution in the states of MA, IL, SC, KY, SC, OH, TN.
Other Recalls by SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION
- Class II: Risk 10/16/2025
- Class II: Risk 09/06/2024
- Class II: Risk 09/06/2024
View all recalls by SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION →
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.