RecallRadar

FDA Device recall Z-2746-2016

The Connecting Bracket (Fixture) Device (1002.65A0) is designed as a connecting element to support ancillary head rests on a Maquet operati…

On 2016-09-14 the FDA classified a Class II recall of The Connecting Bracket (Fixture) Device (1002.65A0) is designed as a connecting element to support ancillary head rests on a Maquet operati… by Maquet Cardiovascular Us Sales, citing 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 Br….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2746-2016
ClassificationClass II
Statusterminated
Initiated2016-08-12
Published2016-09-14
Last updated2026-09-13 11:54 UTC
CompanyMaquet Cardiovascular Us Sales
DistributionUS

Product

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

Reason

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.

Identifiers

code_infoPart Number/Catalog Number 1002.64A0

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2746-2016%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.