United StatesStryker CHROMOPHARE Softlit Ring Surgical Light System (REF: CH00000001; UDI: 07613327296167; all lots, 6,170 units) is affected. It was recalled because the surgical light assembly may not adequately support the weight of the ceiling cover.
What's being recalled
Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001
Recalling firm: Stryker Communications, Flower Mound, TX, United States.
How to identify it
UDI: 07613327296167; All Lots
The hazard
Surgical light assembly may not adequate support the weight of the ceiling cover.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
Worldwide - US Nationwide distribution.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)