FDA recall record

GE Healthcare Discovery PET/CT 710 Product Usage: The systems are intended for head and recall — FDA Z-1746-2019

GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

Class IIclassification
Z-1746-2019official record ID
Jun 26, 2019report date

Recall record at a glance

Official recordZ-1746-2019
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmGE Healthcare, LLC
Report dateJun 26, 2019
Recall initiation dateFeb 12, 2019
Quantity1113 in total
LocationWaukesha, WI, United States

Official product description

Discovery PET/CT 710 Product Usage: The systems are intended for head and whole body attenuation corrected Positron Emission Tomography (PET) imaging and localization of emission activity in patient anatomy by means of integrated PET and CT images.

Why the product was recalled

GE Healthcare PET/CT Table Stop Without Stopping X-Ray Exposure

Distribution information

Nationwide Distribution

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: FDA Mandated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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