Applied Medical Resources Corp: Device Recall
Recall #Z-1010-2026 · 12/11/2025
Class II: Risk
Recall Details
- Recall Number
- Z-1010-2026
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Applied Medical Resources Corp
- Status
- Ongoing
- Date Initiated
- 12/11/2025
- Location
- Rancho Santa Margarita, CA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 450 units
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
Distribution Pattern
US: MI, CA, ME, OUS: France Great Britain, Germany
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.