---
title: "Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23 — FDA record Z-1010-2026 | Is It on Recall"
description: "There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing."
url: https://isitonrecall.com/recall/fda-device-z-1010-2026-kii-low-profile-bladed-dual-pack-qty-1-5x55mm-ref-ctb23/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23 — FDA record Z-1010-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Dec 11, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23
- **Reason**: There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing.
- **Classification**: Class II
- **Recalling firm**: Applied Medical Resources Corp
- **Quantity**: 450 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1010-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1010-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI: (01)00607915126582; Lot # 1546141 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US: MI, CA, ME, OUS: France Great Britain, Germany

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [California](https://isitonrecall.com/state/california/)
- [Maine](https://isitonrecall.com/state/maine/)
- [Michigan](https://isitonrecall.com/state/michigan/)

## Dates in the source

- **Report date**: Jan 14, 2026
- **Recall initiation date**: Dec 11, 2025
- **Center classification date**: Jan 2, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1010-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Applied Medical Resources Corp records](https://isitonrecall.com/brand/applied-medical-resources-corp/)