Baxter recalls iLED 7 surgical lights (models 4068110-4068410) due to reported thermal skin injuries. Affected units have specific serial numbers. Stop using immediately to prevent burns.
Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction due to customer reports of thermal skin injuries when using the iLED 7 surgical light system products listed below. Specific VidiaPort and Trulight product codes are also impacted as they are equipped with iLED 7 light-heads
Baxter is recalling iLED 7 surgical lights that have caused thermal skin injuries. These lights include ceiling, mobile, and pendant models with specific serial numbers. Users should stop using them to avoid burns.
The iLED 7 surgical lights can cause thermal skin injuries when used. This happens because the lights may overheat and burn skin, especially during prolonged use or if the light head is not properly positioned.
Surgical staff and healthcare facilities using the recalled iLED 7 surgical lights are most at risk. Patients and staff could experience burns from improper use.
Check for model numbers 4068110 (ceiling single), 4068120 (mobile), 4068140 (pendant), 4068210 (ceiling duo), 4068310 (ceiling trio), or 4068410 (ceiling quad). Also look for serial numbers starting with UDI/DI 00887761968271 to 00887761968325.
Discontinue use of the recalled iLED 7 surgical lights to prevent thermal skin injuries.
The affected models are iLED 7 surgical lights with model numbers 4068110 (ceiling single), 4068120 (mobile), 4068140 (pendant), 4068210 (ceiling duo), 4068310 (ceiling trio), and 4068410 (ceiling quad).
Check the model number on your light and the serial number, which starts with UDI/DI 00887761968271 to 00887761968325.
Stop using the light immediately to prevent thermal skin injuries. Contact Baxter for further instructions.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-2315-2024 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-2315-2024 from Baxter. 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.
