FDAClass IIAugust 19, 2020

uEXPLORER PET/CT Diagnostic Imaging System - Product recall

uEXPLORER PET/CT Diagnostic Imaging System - Product Usage: This system is intended to be operated by qualified healthcare professionals to assist in…

Why was uEXPLORER PET/CT Diagnostic Imaging System - Product recalled?

1) 1) Potential intermittent issue may cause image data problems, may lead to artifacts; 2) Potential intermittent scout scanning interruption due to angle signal drift caused by external interference; 3) Metal edge overlap of mylar strip in gantry may create sharp edge. May lead to repeat scanning and abrasions.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Serial No. F00002; GTIN 06971576832040

Product
uEXPLORER PET/CT Diagnostic Imaging System - Product Usage: This system is intended to be operated by qualified healthcare professionals to assist in…
Recalling firm
Shanghai United Imaging Healthcare Co., Ltd.
Quantity
1 unit distributed to Texas
Distribution
US Nationwide distribution including in the state of Texas.
Recall date
August 19, 2020
Classification
Class II
Status
Terminated
Agency
FDA (device)
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