FDA recall record

NeuroLogica GM85 Digital Mobile X-ray imaging System recall — FDA Z-0480-2026

The four (4) M5 bolts that secure the Tube Head Unit to the end of the arm may loosen or fracture due to metal fatigue.

Class IIclassification
Z-0480-2026official record ID
Nov 19, 2025report date

Recall record at a glance

Official recordZ-0480-2026
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmNeuroLogica Corporation
Report dateNov 19, 2025
Recall initiation dateOct 7, 2025
Quantity236 units
LocationDanvers, MA, United States

Official product description

GM85 Digital Mobile X-ray imaging System; Model Number: GM85;

Why the product was recalled

The four (4) M5 bolts that secure the Tube Head Unit to the end of the arm may loosen or fracture due to metal fatigue.

Distribution information

Domestic: US Nationwide Distribution. International: Australia, Belgium, Canada, Chile, China Mainland, Czech Republic, Denmark, Ecuador, Finland, France, Germany, GHANA, Hungary, India, Italy, Korea, Malaysia, Mexico, Netherlands, New Zealand, Norway, Peru, Philippines, Poland, Portugal, Saudi Arabia, Serbia, Singapore, Spain, Sweden, Switzerland, Thailand, T¿rkiye, United Kingdom, Utd.Arab Emir., Vietnam,

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.

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