---
title: "Model SM-32HF-Batt; 32KW ANALOG, Mobile X-ray system — FDA record Z-0256-2026 | Is It on Recall"
description: "Sedecal sent an email to its consignees to remind the users that the equipment is not water-resistant and must be cleaned strictly according to the instructions"
url: https://isitonrecall.com/recall/fda-device-z-0256-2026-model-sm-32hf-batt-32kw-analog-mobile-x-ray-system/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Model SM-32HF-Batt; 32KW ANALOG, Mobile X-ray system — FDA record Z-0256-2026

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 Jun 10, 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**: Model SM-32HF-Batt; 32KW ANALOG, Mobile X-ray system
- **Reason**: Sedecal sent an email to its consignees to remind the users that the equipment is not water-resistant and must be cleaned strictly according to the instructions in the manual, clearly outlining the possible consequences of improper cleaning.
- **Classification**: Class II
- **Recalling firm**: SEDECAL SA
- **Quantity**: 22 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0256-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0256-2026%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/DI 08436046001466, Serial Numbers: G-33344, G29404, G29407, G30258, G30236, G63124, G60169, G26234, G26284, G25734, G38069, G-40590, G41143, G62020, G69393, G38082, G41163, G60166, G26244, G40196, G60461, G33309. |

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

## Distribution

US: CA, IL, and NJ

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/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)

## Dates in the source

- **Report date**: Oct 29, 2025
- **Recall initiation date**: Jun 10, 2025
- **Center classification date**: Oct 23, 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-0256-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [SEDECAL SA records](https://isitonrecall.com/brand/sedecal-sa/)