FDAClass IIJanuary 24, 2024

Maquet Blueline Series 30/80 OR Light Systems recall

Maquet Blueline Series 30/80 OR Light Systems, Model Numbers and Catalog Numbers BLUE 30 - ARD569015111A, BLUE 30 - ARD569015111C, BLUE 30…

Why was Maquet Blueline Series 30/80 OR Light Systems recalled?

A potential for a light system to fall in the operating room.

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?

All systems affected

Product
Maquet Blueline Series 30/80 OR Light Systems, Model Numbers and Catalog Numbers BLUE 30 - ARD569015111A, BLUE 30 - ARD569015111C, BLUE 30…
Recalling firm
Getinge Usa Sales Inc
Quantity
236793 units in total
Distribution
US Nationwide. Global Distribution.
Recall date
January 24, 2024
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls