Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23
Reported: January 14, 2026 Initiated: December 11, 2025 #Z-1010-2026
Product Description
Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23
Reason for Recall
There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing.
Details
- Recalling Firm
- Applied Medical Resources Corp
- Units Affected
- 450 units
- Distribution
- US: MI, CA, ME, OUS: France Great Britain, Germany
- Location
- Rancho Santa Margarita, CA
Frequently Asked Questions
What product was recalled? ▼
Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23. Recalled by Applied Medical Resources Corp. Units affected: 450 units.
Why was this product recalled? ▼
There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 14, 2026. Severity: Moderate. Recall number: Z-1010-2026.
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