RecallRadar

FDA Device recall Z-1045-2016

Maquet Getinge Group 1180.19XO Extension Device

On 2016-03-09 the FDA classified a Class II recall of Maquet Getinge Group 1180.19XO Extension Device by Maquet Cardiovascular Us Sales, citing MAQUET Medical Systems USA is initiating a field action for correction of the MAQUET Extension Device (Part No 1180.19F0). The Extension Device is manufactured by Maquet GmbH, in….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1045-2016
ClassificationClass II
Statusterminated
Initiated2016-01-07
Published2016-03-09
Last updated2026-09-13 11:54 UTC
CompanyMaquet Cardiovascular Us Sales
DistributionAZ, MO

Product

Maquet Getinge Group 1180.19XO Extension Device. Manufacturer MAQUET GmbH, Used to support the upper and lower extremities immediately before, during and after fracture surgery. The Extension Device (1180.19F0) is a table top module for use with the Maquet MAGNUS operating table system and it is attached to the base mounting point of the MAGNUS operating table.

Reason

MAQUET Medical Systems USA is initiating a field action for correction of the MAQUET Extension Device (Part No 1180.19F0). The Extension Device is manufactured by Maquet GmbH, in Germany, and is a table top module for use with the Maquet MAGNUS operating table system. Maquet GmbH was made aware of a potential issue that can result in the Extension Device becoming unlocked from the table top, causing it to fall down.

Identifiers

code_infoCatalog Number 1180.19F0; Serial numbers 00003 and 00004.

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-1045-2016%22

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