Trulight 5000/3000 Surgical Light, model numbers: a) 4038210 (Duo Surgical Lights}; b) 4038310 (Trio/Quad Surgical Lights)
FDA Recall Z-2314-2024 · Posted 2024-07-05
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Recalling FirmBaxter Healthcare Corporation
Recall StatusOpen, Classified
Product CodeFTD
Date Initiated2024-06-04
Product Quantity5 units
Reason for Recall
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
Firm Action
Baxter issued an Urgent Medical Device Correction notice to its consignees on 06/04/2024 via US mail, first class. The notice explained the issue with the devices, potential hazards involved, and requested the following:
"Actions to be Taken by Customers:
1. Operators may continue to use the iLED 7 surgical light systems by following
the current instructions for use (IFU) cautions and warnings while considering
the additional information below.
. Utilize the lowest possible illumination level suitable for the procedure,
especially in certain neurological or intestinal procedures on delicate,
thin, dry, or abnormal tissue.
. Avoid overlapping light fields that are set at high intensity (80% or higher).
- If the light intensity of one light-head is set at 80% or higher the
second light-head, if overlapping, should be set at 50% or lower.
- If the light intensity of two or more light heads is set at 80% or
higher, to minimize risk do not overlap them.
. If a very high-intensity setting is temporarily required, reduce intensity as
soon as the need passes.
. Ensure the Adaptive Light Control (ALC) Plus sensor is activated and
indicated on the wall or mobile control panel. If activation of the ALC Plus
is not possible, please contact a technical service representative for
further instructions.
. If the ALC Plus is switched off, the light-head needs to be positioned at
100 centimeters (39.37 inches) from the surgical field. At other distances
the illuminance and irradiance limits can be exceeded, which may result
in thermal skin injuries.
2. Additional safety information reviewing the potential risks of using an overhead
surgical light, including educational safety content is available through Pfiedler
education (a division of AORN) at the URL listed below. This website requires
a one-time registration.
https://www.pfiedlereducation.com/diweb/gateway/f/https*3A*2F*2Fwww.pfi
edlereducation.com*2Fdiweb*2Fcatalog*2Fitem*2Feid*2F1552-2024. "
The notice also requested tha
Root Cause
Under Investigation by firm
Distribution Pattern
Worldwide distribution.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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