Getinge Usa Sales Inc: Medical Device Recall in 2024 - (Recall #: Z-0762-2024)

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 Orchide OR Light Systems, Model Numbers and Catalog Numbers OHDII FHD QL VP01 - ARD568803935, OHDII FHD QL AIR03 U - ARD568803952, OHDII FHD QL AIR03 E - ARD568803967, OHDII FHD QL AIR04 E/U - ARD568803968, OHDII FHD QL+ VP01 - ARD569204944, OHDII AIR03 QL FHD E - ARD568803951

Product Classification:

Class II

Date Initiated: November 8, 2023

Date Posted: January 24, 2024

Recall Number: Z-0762-2024

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 UDI-DI: 3700712415761 3700712415976 3700712418274 3700712418281 3700712412340

Distribution Pattern:

US Nationwide. Global Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated