Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DeltaVision OMX SR Imaging System Model Number: 29115476 The DeltaVision Recalled by GE Healthcare Biosciences Due to Non-conformance with the DeltaVision OMX SR, the interlocks...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact GE Healthcare Biosciences directly.
Affected Products
DeltaVision OMX SR Imaging System Model Number: 29115476 The DeltaVision OMX SR Imaging System is a piece of laboratory equipment for super resolution imaging offluorescently-la beling biological samples. Techniques such as 3D Structured Illumination, Total Internal Reflection Fluorescence and localization microscopy may be used to examine a variety of samples over long periods of time.
Quantity: 39
Why Was This Recalled?
Non-conformance with the DeltaVision OMX SR, the interlocks are not wired in a redundant fashion to make the interlock system single-fault tolerant.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About GE Healthcare Biosciences
GE Healthcare Biosciences has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report