Maquet recalls VOLISTA StandOP surgical lights (model 600) shipped from Oct 2012 to Jun 2017 with keypads that may fail. Affected units have specific serial numbers and part numbers.
Potential keypad failure on VOLISTA StandOP Surgical Lights.
Maquet is recalling VOLISTA StandOP surgical lights (model 600) made between October 2012 and June 2017 that have keypads which could potentially fail. This recall is important because surgical lights are critical during medical procedures, and keypad failures could disrupt operations.
The recall states there is a potential for keypad failure on these surgical lights. While the exact failure mechanism isn't specified, keypad issues could disrupt the light's operation during critical medical procedures, potentially affecting surgical outcomes.
Surgical staff and hospitals that own or use VOLISTA StandOP surgical lights (model 600) from October 2012 to June 2017. Medical professionals using these lights during procedures are most at risk.
Check if your VOLISTA StandOP surgical light (model 600) was shipped between October 2012 and June 2017. Look for specific serial numbers or part numbers listed in the recall notice.
Verify your VOLISTA StandOP surgical light (model 600) was manufactured between October 2012 and June 2017 using the serial numbers or part numbers listed in the recall.
The recall involves VOLISTA StandOP surgical lights (model 600) shipped from October 2012 until June 2017.
Affected part numbers include 568811901, VLT600SF AIM STP; 568811911, VLT600SF AIM STP; 568811961, VLT600DF AIM STP; and others listed in the recall notice.
Check if your light has a serial number from the list provided in the recall (e.g., 38013, 38016, 500641, etc.) or part numbers matching those listed.
We’ve drafted a message you can send Maquet to request your refund or repair — edit it as you like.
Subject: Recall Z-1937-2018 — Maquet Maquet Hello, I own a Maquet that is covered by recall Z-1937-2018 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.
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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.
