FDAClass IIJanuary 24, 2024

Maquet Hanaulux 2006/ 2007 recall

Maquet Hanaulux 2006/ 2007, Blue 100, Blue 130/ 90, Blue Series 30/ 80, and Prismatic OR Light Systems. No Model Numbers.

Why was Maquet Hanaulux 2006/ 2007 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 Hanaulux 2006/ 2007, Blue 100, Blue 130/ 90, Blue Series 30/ 80, and Prismatic OR Light Systems. No Model Numbers.
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)
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