FDAClass IIApril 8, 2026

Stryker CHROMOPHARE Softlit Ring Surgical Light System recall

Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001

Why was Stryker CHROMOPHARE Softlit Ring Surgical Light System recalled?

Surgical light assembly may not adequate support the weight of the ceiling cover.

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?

UDI: 07613327296167; All Lots

Product
Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001
Recalling firm
Stryker Communications
Quantity
6170 units
Distribution
Worldwide - US Nationwide distribution.
Recall date
April 8, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls