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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