Recall
FDAHealthAugust 27, 2025

Vision RT Ltd — The AlignRT InBore system contains six Class 1 lasers which enables the system s cameras to track the patient s position and movement.

⚠️ Vision RT is informing customers of an omission identified in the Instructions for Use for AlignRT InBore systems. Information identifying the lasers and their characteristics was omitted from the Instructions for Use for the subject system as required by 21 CFR 1040,10(h), via conformance with recognized consensus standard IEC 60825-1 Ed. 3 (FDA Laser Notice 56).

Is this relevant to me?

Geography
Unknown
Source agency
FDA
Category
Health
Published
August 27, 2025

U.S. and OUS

What's affected?

Product
The AlignRT InBore system contains six Class 1 lasers which enables the system s cameras to track the patient s position and movement.
Lot code
Part Number V000629

Additional details

Part Number V000629

What should I do?

Recommended action

Class II recall. FDA Mandated Quantity affected: 56.

View original FDA notice →

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