# FDA recall Z-1292-2024

> **SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION** · Class II · device recall initiated 2024-01-29.

## Product

Shimadzu, Trinias, Digital Angiography System

## Reason for recall

Due to capacitor manufacturing issue, their is a potential that Flat Panel Device may have abnormal display or no function.

## Distribution

US Nationwide distribution in the states of OH.

## Key facts

- **Recall number:** Z-1292-2024
- **Recalling firm:** SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-01-29
- **Report date:** 2024-03-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Kyoto, N/A, Japan

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1292-2024

## Citation

> AI Analytics. FDA recall Z-1292-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1292-2024. Source: US FDA. Licensed CC0.

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