FDAClass IIApril 17, 2024

Chromophare Surgical Light System recall

Chromophare Surgical Light System , REF CH00000001

Why was Chromophare Surgical Light System recalled?

Due to insufficient mounting force the stability of surgical light system cannot be guaranteed.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

S/N:03857056/ UDI: 07613327296167

Product
Chromophare Surgical Light System , REF CH00000001
Recalling firm
Stryker Communications
Quantity
1 unit
Distribution
US: None OUS: Chili
Recall date
April 17, 2024
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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