United StatesOlympus Cystoscope Outer Sheath (model/catalog WA22810A; identifier model WA2280A; UDI 04042761051729; all lots), distributed nationwide in the U.S., is affected. It is being removed because it is incompatible when used with a GreenLight Laser for BPH therapy and could damage the device tip.
What's being recalled
Olympus Cystoscope Outer Sheath; Model/Catalog number: WA22810A;
Recalling firm: Olympus Corporation of the Americas, Center Valley, PA, United States.
How to identify it
Model: WA2280A; UDI: 04042761051729; Lot#: All lots;
The hazard
Product being removed due to incompatibility when used in conjunction with a GreenLight Laser for BPH therapy which could damage the tip of the device.
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
Distribution US nationwide.
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)