Maquet Cardiovascular Us Sales, Llc: Medical Device Recall in 2015 - (Recall #: Z-2097-2015)

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:

Magnus Hybrid OR Table Column (1180.01B2) used in conjunction with Siemens Artis Zeego Angiography System. Maquet GmbH & Co.

Product Classification:

Class II

Date Initiated: June 10, 2015

Date Posted: July 29, 2015

Recall Number: Z-2097-2015

Event ID: 71446

Reason for Recall:

There is a potential issue that could result to collision between the C-arm of the angiography system and the MAGNUS OR table system. After switching on the angiography-system, in rare cases, MAGNUS column provides wrong position data for the longitudinal movement leading to a collision.

Status: Terminated

Product Quantity: 12 units

Code Information:

SN 00048

Distribution Pattern:

Worldwide Distribution - US Nationwide Distribution and to the countries of : France, Australia, Belgium, Brazil, Switzerland, Chile, China, Germany, Spain, United Kingdom, Hong Kong, Ireland, Israel, India, Italy, Japan, Kuwait, Kazakhstan, Mexico, Netherlands, Norway, Russia, Sweden, Turkey, Taiwan and South Africa.

Voluntary or Mandated:

Voluntary: Firm initiated