Maquet Cardiovascular Us Sales, Llc: Medical Device Recall in 2016 - (Recall #: Z-2746-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

The Connecting Bracket (Fixture) Device (1002.65A0) is designed as a connecting element to support ancillary head rests on a Maquet operating room table immediately before, during and after surgical interventions as well as for examination and treatment. The fixture is used to adapt a range of different head and horseshoe head rests with a central square mount

Product Classification:

Class II

Date Initiated: August 12, 2016

Date Posted: September 14, 2016

Recall Number: Z-2746-2016

Event ID: 74915

Reason for Recall:

Post Market Surveillance cases reported to Maquet showing instances in which the welded joint between the square mount and the first fixable swivel joint of Maquet's Connecting Bracket (Fixture) Device is broken.

Status: Terminated

Product Quantity: 19 units (US) and 1975 units (OUS)

Code Information:

Part Number/Catalog Number 1002.64A0

Distribution Pattern:

Nationwide Distribution to CA, FL, IA, IN, MO, UT and WI

Voluntary or Mandated:

Voluntary: Firm initiated