FDA recall record

GE Medical Systems Imactis CT-Navigation System, stereotaxic accessory for Computer recall — FDA Z-1590-2026

There is a potential issue that can lead to discordance between the simulated needle trajectory/tip position and the actual needle trajectory/tip position.

Class IIclassification
Z-1590-2026official record ID
Apr 1, 2026report date

Recall record at a glance

Official recordZ-1590-2026
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmGE Medical Systems, LLC
Report dateApr 1, 2026
Recall initiation dateFeb 3, 2026
Quantity125 units
LocationWaukesha, WI, United States

Official product description

Imactis CT-Navigation System, stereotaxic accessory for Computer Tomography (CT), systems, Model Numbers E85101LA and E85101LP

Why the product was recalled

There is a potential issue that can lead to discordance between the simulated needle trajectory/tip position and the actual needle trajectory/tip position.

Distribution information

Worldwide distribution - US Nationwide.

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: Voluntary: Firm initiated. 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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