Getinge Usa Sales Inc: Medical Device Recall in 2024 - (Recall #: Z-0771-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: November 8, 2023

Date Posted: January 24, 2024

Recall Number: Z-0771-2024

Event ID: 93567

Reason for Recall:

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

Status: Ongoing

Product Quantity: 236793 units in total

Code Information:

All systems affected

Distribution Pattern:

US Nationwide. Global Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated