Maquet SAS Recalls

Overview of recall records associated with Maquet SAS, including dates, categories and classifications where available.

2recall records

Jul 25, 2018latest record date

Jun 6, 2018earliest record date

Recall history in this database

Classification mix: Class II: 2.

Medical DeviceJul 25, 2018

Maquet SAS VOLISTA StandOP Surgical Light, ARD568811961 VLT600DF AIM STP recall — FDA Z-2502-2018

Certain VOLISTA StandOP Surgical Lights have been identified as having a potential light head detachment issue. Improper assembly of the bracket that connects the light head to the axle…

Class IIFDA: TerminatedMaquet SAS

Medical DeviceJun 6, 2018

Maquet SAS VOLISTA StandOP (model 600) surgical lights shipped from October 2012 until June recall — FDA Z-1937-2018

Potential keypad failure on VOLISTA StandOP Surgical Lights.

Class IIFDA: TerminatedMaquet SAS

Understanding this recall history

This page summarizes recall records in which the official source identifies Maquet SAS as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.