FDA Device recall Z-1292-2024
Shimadzu, Trinias, Digital Angiography System
- FDA Device
- Class II
- ongoing
- Published 2024-03-20
On 2024-03-20 the FDA classified a Class II recall of Shimadzu, Trinias, Digital Angiography System by Shimadzu Medical Systems Division, citing due to capacitor manufacturing issue, their is a potential that Flat Panel Device may have abnormal display or no function.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1292-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-01-29 |
| Published | 2024-03-20 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Shimadzu Medical Systems Division |
| Distribution | US |
Product
Shimadzu, Trinias, Digital Angiography System
Reason
Due to capacitor manufacturing issue, their is a potential that Flat Panel Device may have abnormal display or no function.
Identifiers
| code_info | Serial Number: 41EFFF7D3001/UDI: (01)04540217058020 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1292-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.