Mizuho America, Inc.: Medical Device Recall in 2020 - (Recall #: Z-0567-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: September 11, 2019

Date Posted: December 23, 2020

Recall Number: Z-0567-2021

Event ID: 85442

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.

Status: Ongoing

Product Quantity: 10

Code Information:

Tilt Movement-Leaking Valve (7300BX-18-351-70) serial numbers: MUC-20163-0001, MUC-2016Z-0002, MUC-2016Z-0003, MUC-20177-0005, MUC-20177-0007, MUC-20177-0008, MUC-20177-0009, MUC-20189-0017 & MUC-2018Y-0018. Unintended movement due to infrared signal errors (7300BX-18-351-70) serial numbers: MUC-20163-0001, MUC-2016Z-0002, MUC-2016Z-0003, MUC-20177-0005, MUC-20177-0007, MUC-20177-0008, MUC-20177-0009, MUC-20189-0017, MUC-2018Y-0018 & MUC-2018Y-0019.

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated