Maquet Medical Systems USA: Medical Device Recall in 2015 - (Recall #: Z-0993-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

TEGRIS System manufactured by MAQUET GMBH in Germany The Maquet Tegris OR Integration System is designed to be used as the central operating unit in an operating room. The integration system has two main functions: Recording and distribution of images and videos and interaction with medical and non-medical devices.

Product Classification:

Class II

Date Initiated: August 21, 2014

Date Posted: January 28, 2015

Recall Number: Z-0993-2015

Event ID: 69560

Reason for Recall:

The wrong movement results on the MAGNUS OR table. The button commands on the TEGRIS touchscreen for Lower Leg Up and Upper Leg Down are switched in the software for the integration with the MAGNUS operating table system.

Status: Terminated

Product Quantity: 6 units

Code Information:

part number: 1703.35AO, with software version up to 2.1.x.x.

Distribution Pattern:

US Nationwide Distribution including NE, NY and PA.

Voluntary or Mandated:

Voluntary: Firm initiated