FDAClass IIJuly 3, 2024

MULTIX TOP - Intended Use: The Multix TOP I PRO recall

MULTIX TOP - Intended Use: The Multix TOP I PRO Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP…

Why was MULTIX TOP - Intended Use: The Multix TOP I PRO recalled?

Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI-DI: N/A Serial Numbers: 1523 1585 1897

Product
MULTIX TOP - Intended Use: The Multix TOP I PRO Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP…
Recalling firm
Siemens Medical Solutions USA, Inc
Quantity
3 units
Distribution
US Nationwide distribution.
Recall date
July 3, 2024
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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