---
title: "Brand Name: TruScan Body, REF CN38-SB Product Name: TruScan Body compatible w... — FDA record Z-1313-2025 | Is It on Recall"
description: "Retroactive: Due to defect and quality issues dental scanner may not scan properly/accurately"
url: https://isitonrecall.com/recall/fda-device-z-1313-2025-brand-name-truscan-body-ref-cn38-sb-product-name-truscan-body-compatible-with-conelog-3-8-model-cata/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Brand Name: TruScan Body, REF CN38-SB Product Name: TruScan Body compatible with CONELOG 3.8 Model/Catalog Number: CN... — FDA record Z-1313-2025

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 27, 2023. 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**: Brand Name: TruScan Body, REF CN38-SB Product Name: TruScan Body compatible with CONELOG 3.8 Model/Catalog Number: CN38-SB Software Version: N/A
- **Reason**: Retroactive: Due to defect and quality issues dental scanner may not scan properly/accurately
- **Classification**: Class II
- **Recalling firm**: TruAbutment Inc.
- **Quantity**: 61 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1313-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1313-2025%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 | Lot Code: KCCBB1216110/ UDI: (01)08800076411791 |

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

## Distribution

US: CA, CO, FL, GA, IA, IL, MD, MN, MS, OH, OR, SD, UT, VA, WA, WI OUS: Japan, Great Britain , Canada

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/)
- [Colorado](https://isitonrecall.com/state/colorado/)
- [Florida](https://isitonrecall.com/state/florida/)
- [Georgia](https://isitonrecall.com/state/georgia/)
- [Iowa](https://isitonrecall.com/state/iowa/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Maryland](https://isitonrecall.com/state/maryland/)
- [Minnesota](https://isitonrecall.com/state/minnesota/)
- [Mississippi](https://isitonrecall.com/state/mississippi/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Oregon](https://isitonrecall.com/state/oregon/)
- [South Dakota](https://isitonrecall.com/state/south-dakota/)
- [Utah](https://isitonrecall.com/state/utah/)
- [Virginia](https://isitonrecall.com/state/virginia/)
- [Washington](https://isitonrecall.com/state/washington/)
- [Wisconsin](https://isitonrecall.com/state/wisconsin/)

## Dates in the source

- **Report date**: Mar 19, 2025
- **Recall initiation date**: Dec 27, 2023
- **Center classification date**: Mar 11, 2025

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-1313-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [TruAbutment Inc. records](https://isitonrecall.com/brand/truabutment-inc/)