CLASS II ONGOING Device recall · Reported 29 Oct 2025 · FDA Enforcement Report

Shanghai United Imaging Healthcare Co., Ltd recalled by UIH Technologies

UIH Technologies is recalling Shanghai United Imaging Healthcare Co., Ltd. The recall was initiated on 12 Sep 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesUDI: (01)06971576832040; Serial Number: F00002, F00015
Quantity recalled2 UNITS

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-0222-2026
FDA event ID
97668
Recalling firm
UIH Technologies, Houston, TX
Classification
Class II
Status
Ongoing
Recall initiated
12 Sep 2025
FDA classified
21 Oct 2025
Reported
29 Oct 2025
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons

Timeline

12 Sep 2025Recall initiated by company
21 Oct 2025Classified by FDA+39 days
29 Oct 2025Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.

Product as listed by the FDA

Shanghai United Imaging Healthcare Co., Ltd. Positron Emission Tomography and Computed Tomography System Model:uEXPLORER MD, Rx Only

Where it was distributed

US: OUS:

Questions about this recall

Is Shanghai United Imaging Healthcare Co., Ltd recalled?

Yes. UIH Technologies recalled Shanghai United Imaging Healthcare Co., Ltd on 12 Sep 2025. The recall is Class II and its status is Ongoing. Recall number Z-0222-2026.

Why was it recalled?

Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.

Which lots are affected?

UDI: (01)06971576832040; Serial Number: F00002, F00015

Where was it sold?

US: OUS:

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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