← FDA ENFORCEMENT
Z-1010-2026Class II
Applied Medical Resources Corp
What this record is not
A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.
Recalling firm
Applied Medical Resources Corp
Product type
Device
Status
Ongoing
Report date
2026-01-14
Distribution
US: MI, CA, ME, OUS: France Great Britain, Germany
Firm state
CA
Product quantity
450 units
Initiated by
Voluntary: Firm initiated
Reason for recall
There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing.
Product description
Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23
Code / lot info
UDI: (01)00607915126582; Lot # 1546141
Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →