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Maquet SAS recalls

Maquet SAS has 2 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 25 Jul 2018. The most frequent reason is device malfunction.

Total recalls2since 2018

Last 12 months0reported

Class I00% of total

Ongoing0latest 25 Jul 2018

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 2 100%Class III 0 0%

Why maquet sas is recalled

Device Malfunction2100%

Product types

Surgical Instruments150%
Hip & Knee Implants150%

By year

20182100%

All maquet sas recalls, newest first

2 total

Reported	Class	Recall	Company	Reason	Where
25 Jul 2018Device	CLASS II	Volista StandOP Surgical Light, ARD568811961 VLT600DF AIM STP recalled	Maquet SAS	Device Malfunction	Nationwide
6 Jun 2018Device	CLASS II	Volista StandOP recalled by Maquet SAS	Maquet SAS	Device Malfunction	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.