Mizuho America recalls Microsurgical Operating Room Tables 7300BX with serial numbers MUC-20163-0001 to MUC-2018Y-0019 due to unintended tilting and infrared signal errors that could cause incorrect operation.
Unintended tilting of the Tabletop MST 7300BX and incorrect operation due to infrared operating signal errors of Tabletops MST 7300B and MST 7300BX.
Mizuho America is recalling Microsurgical Operating Room Tables 7300BX with specific serial numbers because they can tilt unexpectedly or malfunction due to infrared signal errors. This could lead to incorrect surgical procedures if the table moves during operations.
The tables can tilt unexpectedly due to infrared signal errors, which may cause incorrect operation during surgery. This could lead to surgical errors if the table moves while a procedure is ongoing.
Surgical teams using the Microsurgical Operating Room Tables 7300BX with the listed serial numbers are most at risk. Patients and staff during surgery could be affected if the table tilts unexpectedly.
Check for serial numbers starting with MUC-20163-0001 through MUC-2018Y-0019 on the Microsurgical Operating Room Tables 7300BX. The specific model is the 7300BX with the serial numbers listed in the recall notice.
Look for serial numbers starting with MUC-20163-0001 through MUC-2018Y-0019 on the table's label.
The Microsurgical Operating Room Tables 7300BX with serial numbers MUC-20163-0001 to MUC-2018Y-0019.
The tables can tilt unexpectedly or malfunction due to infrared signal errors, which could cause incorrect operation during surgery.
The recall record does not mention a remedy or fix for the issue.
We’ve drafted a message you can send Mizuho America to request your refund or repair — edit it as you like.
Subject: Recall Z-0567-2021 — Mizuho America Mizuho America Hello, I own a Mizuho America that is covered by recall Z-0567-2021 from Mizuho America. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
