# FDA recall Z-0567-2021

> **Mizuho America, Inc.** · Class II · device recall initiated 2019-09-11.

## Product

Microsurgical Operating Room Tables;7300BX (18-351-70).

## Reason for recall

Unintended tilting of the Tabletop MST 7300BX and incorrect operation due to infrared operating signal errors of Tabletops MST 7300B and MST 7300BX.

## Distribution

US: AZ, CA, FL, MO, NC, OH, PA, TX, and WI.  OUS: Greece, Israel, Japan, and Ukraine.

## Key facts

- **Recall number:** Z-0567-2021
- **Recalling firm:** Mizuho America, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2019-09-11
- **Report date:** 2020-12-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Union City, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0567-2021

## Citation

> AI Analytics. FDA recall Z-0567-2021. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-0567-2021. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*