Recall Register

Device recall: uCT 530 Computed Tomography X-Ray System

Class II FDA enforcement event 85809. Recall start date: . Status in the FDA record: Ongoing.

Reason for recall, in the words of FDA

Two issues were identified with the computed tomography x-ray system including a service function which may cause false marking of a bad channel resulting in ring artifacts, and potential intermittent scout scanning interruption due to occasional angle signal drift.. If these problems occur, it may be necessary to rescan the patient resulting in an additional dose of radiation and the possible…

Class II, in the words of FDA

a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote

Shanghai United Imaging Healthcare Co., Ltd. started this device recall on 8 May 2020. The firm address in the FDA record is in Shanghai. FDA put the recall in Class II. FDA event 85809 has 1 product record. The first FDA enforcement report date is 8 Jul 2020. The record gives the status Ongoing.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

Distributed to Texas.

Recalling firm

Shanghai United Imaging Healthcare Co., Ltd., Shanghai, N/A, China.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

1 product record in the event.

FDA event 85809: product records
Recall numberProductQuantityClassStatusReport date
Z-2472-2020uCT 530 Computed Tomography X-Ray System4 unitsClass IIOngoing8 Jul 2020

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class II: The middle of the three FDA recall classes.

The event in context

Device events that started in 2020
916
Share of these events in Class II
93%
Product records in this event
1Median of the firm: 1
Events of the firm on the register
14

Other events of the firm

Other FDA enforcement events of Shanghai United Imaging Healthcare Co., Ltd.
InitiatedProduct (first record)TypeClassRecords
1 Mar 2023Shanghai United Imaging Healthcare Co., Ltd. Positron Emission Tomography (PET) and Computed Tomography (CT), Model uMI DeviceClass II1
30 May 2022Positron Emission Tomography and Computed Tomography System, Model: uMI 550DeviceClass II1
2 Aug 2021uMI 550 System - Product Usage: intended to be operated by qualified healthcare professionals to assist in the detectionDeviceClass II2
25 Jan 2021Digitial Medica X-ray Imagining System, Model: uDR 596i, RX, CE0123, UDI:(01) 06971576833023 - Product Usage: intended tDeviceClass II1
5 Aug 2020Computed Tomography X-Ray System, Model uCT 530, Rx, CE, GTIN: 06971576831012 - Product Usage: ntended to produce cross-DeviceClass II4
16 Jul 2020uEXPLORER PET/CT Diagnostic Imaging System - Product Usage: This system is intended to be operated by qualified healthcaDeviceClass II2
20 Jun 2020Computed Tomography X-ray System; Model uCT 760; Rx; UDI: (01) GTIN: 06971576831043 - Product Usage: intended to produceDeviceClass II3
23 May 2020Computed Tomography X-ray System, Model: uCT 550, GTIN: 06971576831036 Intended use The uCT Computed Tomography X-ray SyDeviceClass II1
8 May 2020uCT 760 System, Computed Tomography X-ray SystemDeviceClass II1
26 Mar 2020Positron Emission Tomography and Computed Tomography System, Model: uMI 550, Material Number: 88000057 - Product Usage: DeviceClass II1

Shanghai United Imaging Healthcare Co., Ltd.: all 14 events

Official channels

Cite this page

Recall Register. FDA enforcement event 85809. https://recallregister.com/fda/ii/85809/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA device enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: Distributed to Texas.
What quantity of product is in FDA event 85809?
The FDA record gives this quantity: 4 units
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many device recalls of 2020 have the same class?
93% of the 916 device events that started in 2020 are in Class II.