RecallRadar

FDA Device recall Z-0567-2021

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

On 2020-12-23 the FDA classified a Class II recall of Microsurgical Operating Room Tables;7300BX (18-351-70) by Mizuho America, citing unintended tilting of the Tabletop MST 7300BX and incorrect operation due to infrared operating signal errors of Tabletops MST 7300B and MST 7300BX.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0567-2021
ClassificationClass II
Statusongoing
Initiated2019-09-11
Published2020-12-23
Last updated2026-09-13 11:55 UTC
CompanyMizuho America
DistributionAZ, CA, FL, MO, NC, OH, PA, TX, WI

Product

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

Reason

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

Identifiers

code_info
Tilt Movement-Leaking Valve (7300BX-18-351-70) serial numbers: MUC-20163-0001, MUC-2016Z-0002, MUC-2016Z-0003, MUC-2017…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.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0567-2021%22

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