Baxter recalls Trulight 5000/3000 surgical lights with specific model numbers due to reported thermal skin injuries. Affected units include Duo and Trio/Quad models with listed serial numbers.
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 Trulight 5000/3000 surgical lights that have been reported to cause thermal skin injuries. This recall affects specific model numbers and serial numbers used in surgical settings.
The iLED 7 surgical light system in these products has been reported to cause thermal skin injuries when used. This occurs due to overheating of the light head, which can lead to burns on the skin.
Surgical teams and healthcare facilities using the recalled Trulight 5000/3000 surgical lights with model numbers 4038210 or 4038310 are most at risk. Patients and staff during procedures may experience thermal skin injuries.
Check for model numbers 4038210 (Duo Surgical Lights) or 4038310 (Trio/Quad Surgical Lights). Affected units have specific serial numbers: 107565745 for model 4038210 and 107565746, 107592673, 107592675, 108034069 for model 4038310.
Identify if your Trulight 5000/3000 surgical light has model numbers 4038210 or 4038310.
Reach out to Baxter Healthcare Corporation for assistance with the recall process.
The iLED 7 surgical light system has been reported to cause thermal skin injuries due to overheating of the light head.
Model numbers 4038210 (Duo Surgical Lights) and 4038310 (Trio/Quad Surgical Lights).
Check for model numbers 4038210 or 4038310 with specific serial numbers listed in the recall notice.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-2314-2024 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-2314-2024 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.
