FDA Device recall Z-1937-2018

VOLISTA StandOP (model 600) surgical lights shipped from October 2012 until June 2017 equipped with keypads with Ref

FDA Device
Class II
terminated
Published 2018-06-06

On 2018-06-06 the FDA classified a Class II recall of VOLISTA StandOP (model 600) surgical lights shipped from October 2012 until June 2017 equipped with keypads with Ref by Maquet Sas, citing potential keypad failure on VOLISTA StandOP Surgical Lights.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1937-2018
Classification	Class II
Status	terminated
Initiated	2018-04-19
Published	2018-06-06
Last updated	2026-09-13 11:54 UTC
Company	Maquet Sas
Distribution	US

Product

VOLISTA StandOP (model 600) surgical lights shipped from October 2012 until June 2017 equipped with keypads with Ref. ARD568801560; Part numbers: 568811901, VLT600SF AIM STP; 568811911, VLT600SF AIM STP; 568811961, VLT600DF AIM STP; 568821910, VLT600SF STP QL; 568821911, VLT600SF AIM STP QL; 568821960, VLT600DF STP QL; 568821961, VLT600DF AIM STP QL VOLISTA surgical lights are intended to be used to provide visible illumination of the surgical area or patient during surgical operations, diagnostics and treatment.

Reason

Potential keypad failure on VOLISTA StandOP Surgical Lights.

Identifiers

code_info	Serial Numbers: 38013 38016 500641 500644 25002 35025 35028 38012 38015 500000 500001 500003 500004 50001… Serial Numbers: 38013 38016 500641 500644 25002 35025 35028 38012 38015 500000 500001 500003 500004 500014 500015 500016 500018 500037 500039 500020 500060 500063 500642 500643 31053 500058 38009 38026 31002 31030 31048 31054 21001 21002 35024 35012 35013 35014 35015 38017 500001 500017 35029 35017 35027 31019 31020 31022 31024 31025 31026 31000 31000 31001 31002 31003 31006 31009 31010 31012 31008 31047 31050 31051 31052 500002 500060 500061 500072 500073 500680 500685 500686 500687 500692 510082 500062 500064 500042 500044 31012 31013 31014 31020 38011 38014 31006 31008 31015 31016 500068 500070 500071 500074 31021 31023 38018 38019 38020 38021 38022 38023 38024 38025 31004 35011 31004 31017 31018 35000 35001 35018 35019 35020 35021 35022 35023 35026 35030 35031 35032 35033 38027 31001 31003 28003 28004 25005 25006 500055 500059 500011 500013 25007 25

code_info

Serial Numbers: 38013 38016 500641 500644 25002 35025 35028 38012 38015 500000 500001 500003 500004 50001…

Serial Numbers: 38013 38016 500641 500644 25002 35025 35028 38012 38015 500000 500001 500003 500004 500014 500015 500016 500018 500037 500039 500020 500060 500063 500642 500643 31053 500058 38009 38026 31002 31030 31048 31054 21001 21002 35024 35012 35013 35014 35015 38017 500001 500017 35029 35017 35027 31019 31020 31022 31024 31025 31026 31000 31000 31001 31002 31003 31006 31009 31010 31012 31008 31047 31050 31051 31052 500002 500060 500061 500072 500073 500680 500685 500686 500687 500692 510082 500062 500064 500042 500044 31012 31013 31014 31020 38011 38014 31006 31008 31015 31016 500068 500070 500071 500074 31021 31023 38018 38019 38020 38021 38022 38023 38024 38025 31004 35011 31004 31017 31018 35000 35001 35018 35019 35020 35021 35022 35023 35026 35030 35031 35032 35033 38027 31001 31003 28003 28004 25005 25006 500055 500059 500011 500013 25007 25

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-1937-2018%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.