Reported Jan 14, 2026 · Ongoing
Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23
Applied Medical Resources Corp.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Applied Medical Resources Corp · 22872 Avenida Empresa · Rancho Santa Margarita, CA · 92688-2650
Is this the product you have?
- Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm
- REFCTB23
- Lot codes and dates
- UDI
(01)00607915126582Lot # 1546141
- UDI
- Amount recalled
- 450 units
Where it was sold
Why it was recalled
There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing.
This product could cause temporary or reversible health problems — stop using it.
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