GE Healthcare Biosciences DeltaVision OMX SR Imaging System recall — FDA Z-0388-2019
Non-conformance with the DeltaVision OMX SR, the interlocks are not wired in a redundant fashion to make the interlock system single-fault tolerant.
Overview of recall records associated with GE Healthcare Biosciences, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Non-conformance with the DeltaVision OMX SR, the interlocks are not wired in a redundant fashion to make the interlock system single-fault tolerant.
This page summarizes recall records in which the official source identifies GE Healthcare Biosciences as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.