Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
VOLISTA StandOP (model 600) surgical lights shipped from October 2012 Recalled by Maquet SAS Due to Potential keypad failure on VOLISTA StandOP Surgical Lights.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Maquet SAS directly.
Affected Products
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.
Quantity: 187
Why Was This Recalled?
Potential keypad failure on VOLISTA StandOP Surgical Lights.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Maquet SAS
Maquet SAS has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report