United StatesKii Low Profile, Bladed Dual Pack, Qty. 1 5x55mm (REF: CTB23; UDI: (01)00607915126582; Lot #1546141) is recalled and was distributed in the U.S. (MI, CA, ME) and internationally (France, Great Britain, Germany). The firm recalled the device because there is the potential for extended length of the blade obturator after assembly into the cannula and seal housing.
What's being recalled
Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23
Recalling firm: Applied Medical Resources Corp, Rancho Santa Margarita, CA, United States.
How to identify it
UDI: (01)00607915126582; Lot # 1546141
The hazard
There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing.
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
US: MI, CA, ME, OUS: France Great Britain, Germany
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)