Baxter Healthcare recalls VidiaPort carrying arms for surgical lights due to reported thermal skin injuries. Affected models include ceiling single, duo, and trio surgical lights with specific 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 Healthcare is recalling VidiaPort carrying arms for certain ceiling surgical lights after customer reports of thermal skin injuries. This recall affects specific model numbers and serial numbers listed in the notice.
The VidiaPort carrying arms are equipped with iLED 7 light-heads that have been reported to cause thermal skin injuries when used. This risk occurs during normal surgical lighting operations.
Surgical staff and healthcare facilities using the recalled VidiaPort carrying arms with iLED 7 surgical lights. Those with the specific model numbers and serial numbers listed are most at risk.
Check if your VidiaPort carrying arm has model numbers 4028110 (Ceiling Single Surgical Light), 4028210 (Ceiling Duo Surgical Lights), or 4028310 (Ceiling Trio Surgical Lights). Also check the UDI/DI and serial numbers listed in the recall notice.
If you have experienced skin injuries from the surgical light, contact Baxter Healthcare immediately.
Confirm your VidiaPort carrying arm model number matches the recalled types: 4028110, 4028210, or 4028310.
Reach out to Baxter Healthcare for assistance with the recall using the provided serial numbers or model information.
The recall affects VidiaPort carrying arms with model numbers 4028110 (Ceiling Single Surgical Light), 4028210 (Ceiling Duo Surgical Lights), and 4028310 (Ceiling Trio Surgical Lights).
Check the model number and serial numbers listed in the recall notice. Affected units have specific UDI/DI and serial numbers provided in the record.
Yes, customer reports indicate thermal skin injuries can occur when using the iLED 7 surgical light system with the recalled VidiaPort carrying arms.
We’ve drafted a message you can send Baxter Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-2313-2024 — Baxter Healthcare Baxter Healthcare Hello, I own a Baxter Healthcare that is covered by recall Z-2313-2024 from Baxter Healthcare. 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.
