Class II — Mizuho America, Inc.
| Recalling firm | MIZUHO AMERICA, INC. |
|---|---|
| Registered facility | MIZUHO AMERICA, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Unintended tilting of the Tabletop MST 7300BX and incorrect operation due to infrared operating signal errors of Tabletops MST 7300B and MST 7300BX. |
| Product | Microsurgical Operating Room Tables;7300BX (18-351-70). |
| Quantity | 10 |
| Distribution | US: AZ, CA, FL, MO, NC, OH, PA, TX, and WI. OUS: Greece, Israel, Japan, and Ukraine. |
| Initiated | 2019-09-11 |
| Classified | 2020-12-14 |
| Recall number | Z-0567-2021 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Mizuho America, Inc. (Z-0567-2021).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/85442/
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