Kii Low Profile recall
Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23
Why was Kii Low Profile recalled?
There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI: (01)00607915126582; Lot # 1546141
- Product
- Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23
- Recalling firm
- Applied Medical Resources Corp
- Quantity
- 450 units
- Distribution
- US: MI, CA, ME, OUS: France Great Britain, Germany
- Recall date
- January 14, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)