Health product recall

Iled 7 Surgical Light System

Last updated

Summary

Product
Iled 7 Surgical Light System
Issue
Medical devices - Labelling and packaging
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalogue number

Iled 7

All lots.

4068140
4068310
4068410
4068110
4068120
4068210

Vidiaport Ceiling Duo Surgical Lights, Vidiaport Ceiling Trio Surgical Lights

More than 10 numbers, contact manufacturer.

4028210
4028310

Issue

Baxter 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.

Recall start date: June 10, 2024

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Dental
Health products - Medical devices - General and plastic surgery
Companies
Baxter Medical Systems Gmbh T Co. Kg
Karl-Zeiss-Str. 7-9, Saalfeld, Germany, 07318
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-75724

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