---
title: "Shanghai United Imaging Healthcare Co., Ltd. Positron Emission Tomography and... — FDA record Z-0222-2026 | Is It on Recall"
description: "Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement."
url: https://isitonrecall.com/recall/fda-device-z-0222-2026-shanghai-united-imaging-healthcare-co-ltd-positron-emission-tomography-and-computed-tomography-syste/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Shanghai United Imaging Healthcare Co., Ltd. Positron Emission Tomography and Computed Tomography System Model:uEXPLO... — FDA record Z-0222-2026

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 Sep 12, 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**: Shanghai United Imaging Healthcare Co., Ltd. Positron Emission Tomography and Computed Tomography System Model:uEXPLORER MD, Rx Only
- **Reason**: Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
- **Classification**: Class II
- **Recalling firm**: UIH Technologies LLC
- **Quantity**: 2 UNITS
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0222-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0222-2026%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)06971576832040; Serial Number: F00002, F00015 |

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

## Distribution

US: OUS:

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Oct 29, 2025
- **Recall initiation date**: Sep 12, 2025
- **Center classification date**: Oct 21, 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-0222-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [UIH Technologies LLC records](https://isitonrecall.com/brand/uih-technologies-llc/)