---
title: "NanoZoomer S360MD Slide scanner system-automated system for creating, viewing... — FDA record Z-2280-2023 | Is It on Recall"
description: "If the wrong barcode information is recorded in the NDPi file, a pathologist may refer to the whole slide image (WSI) of a different patient."
url: https://isitonrecall.com/recall/fda-device-z-2280-2023-nanozoomer-s360md-slide-scanner-system-automated-system-for-creating-viewing-and-managing-digital-sl/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# NanoZoomer S360MD Slide scanner system-automated system for creating, viewing, and managing digital slides. The NanoZ... — FDA record Z-2280-2023

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 Jun 6, 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**: NanoZoomer S360MD Slide scanner system-automated system for creating, viewing, and managing digital slides. The NanoZoomer System creates diagnostic-quality digital images of glass slides containing formalin-fixed paraffin-embedded (FFPE) tissue. Catalog Number: C13220-01MD
- **Reason**: If the wrong barcode information is recorded in the NDPi file, a pathologist may refer to the whole slide image (WSI) of a different patient.
- **Classification**: Class II
- **Recalling firm**: Hamamatsu Corporation
- **Quantity**: 1 unit
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2280-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2280-2023%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-DI: 010458238901065911220 S/N: 90121100033 |

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

## Distribution

NY

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

- [New York](https://isitonrecall.com/state/new-york/)

## Dates in the source

- **Report date**: Aug 9, 2023
- **Recall initiation date**: Jun 6, 2023
- **Center classification date**: Jul 31, 2023

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-2280-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Hamamatsu Corporation records](https://isitonrecall.com/brand/hamamatsu-corporation/)