FDA recall record

Mizuho Microsurgical Operating Room Tables;7300B (18-350-70) recall — FDA Z-0566-2021

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

Class IIclassification
Z-0566-2021official record ID
Dec 23, 2020report date

Recall record at a glance

Official recordZ-0566-2021
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmMizuho America, Inc.
Report dateDec 23, 2020
Recall initiation dateSep 11, 2019
Quantity8
LocationUnion City, CA, United States

Official product description

Microsurgical Operating Room Tables;7300B (18-350-70);

Why the product was recalled

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

Distribution information

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

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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