PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: January 24, 2024 Initiated: November 8, 2023 #Z-0771-2024

Product Description

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

Reason for Recall

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

Details

Recalling Firm
Getinge Usa Sales Inc
Units Affected
236793 units in total
Distribution
US Nationwide. Global Distribution.
Location
Wayne, NJ

Frequently Asked Questions

What product was recalled?
Maquet Hanaulux 2006/ 2007, Blue 100, Blue 130/ 90, Blue Series 30/ 80, and Prismatic OR Light Systems. No Model Numbers.. Recalled by Getinge Usa Sales Inc. Units affected: 236793 units in total.
Why was this product recalled?
A potential for a light system to fall in the operating room.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 24, 2024. Severity: Moderate. Recall number: Z-0771-2024.