Maquet recalls VOLISTA StandOP Surgical Lights with serial numbers 31000-38027 due to potential light head coating cracks that could cause surgical field contamination and patient infection.
Potential that the coating of the light head forks on the VOLISTA Surgical Lights may crack, posing the risk of particles falling into the surgical field during surgery that may result in patient infection
Maquet is recalling VOLISTA StandOP Surgical Lights with specific serial numbers because the light head coating may crack during surgery, risking particles falling into the surgical field and causing patient infections. This is a serious safety issue for surgical procedures.
The coating on the light head forks of these surgical lights may crack during use. If cracked, small particles could fall into the surgical field, potentially causing infections in patients during surgery.
Surgical teams using the recalled VOLISTA StandOP Surgical Lights with serial numbers starting with 31000-38027 are most at risk. Patients undergoing surgery with these lights could face infection from particles falling into the surgical field.
Check if your VOLISTA StandOP Surgical Light has a serial number starting with 31000, 31001, 31002, 31003, 31004, 31006, 31008, 31009, 31010, 31012, 31017, 31018, 31019, 31020, 31021, 31022, 31023, 31024, 31025, 31026, 35000, 35001, 35011, 35012, 35013, 35014, 35015, 35017, 35018, 35019, 35020, 35021, 35022, 35023, 35024, 35025, 35026, 35027, 35028, 35030, 35031, 35032, 35033, 38000, 38001, 38002, 38003, 38009, 38011, 38012, 38013, 38014, 38015, 38016, 38018, 38019, 38020, 38021, 38022, 38023, 38025, 38026, 38027.
Identify if your VOLISTA StandOP Surgical Light has a serial number starting with 31000-38027 as listed in the recall.
The coating on the light head forks may crack during surgery, potentially causing particles to fall into the surgical field and result in patient infections.
Check if your VOLISTA StandOP Surgical Light has a serial number starting with 31000, 31001, 31002, 31003, 31004, 31006, 31008, 31009, 31010, 31012, 31017, 31018, 31019, 31020, 31021, 31022, 31023, 31024, 31025, 31026, 35000, 35001, 35011, 35012, 35013, 35014, 35015, 35017, 35018, 35019, 35020, 35021, 35022, 35023, 35024, 35025, 35026, 35027, 35028, 35030, 35031, 35032, 35033, 38000, 38001, 38002, 38003, 38009, 38011, 38012, 38013, 38014, 38015, 38016, 38018, 38019, 38020, 38021, 38022, 38023, 38025, 38026, or 38027.
The recall does not specify a remedy, so contact Maquet directly for guidance on next steps.
We’ve drafted a message you can send Maquet to request your refund or repair — edit it as you like.
Subject: Recall Z-1854-2019 — Maquet Maquet Hello, I own a Maquet that is covered by recall Z-1854-2019 from Maquet. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
