GE Healthcare Biosciences recalls DeltaVision OMX SR Imaging System model 29115476 due to non-redundant interlock wiring, which could lead to system malfunctions. Affected users should contact for details.
Non-conformance with the DeltaVision OMX SR, the interlocks are not wired in a redundant fashion to make the interlock system single-fault tolerant.
GE Healthcare Biosciences is recalling the DeltaVision OMX SR Imaging System model 29115476 because its interlock system isn't wired redundantly. This could cause the system to malfunction during use, potentially leading to safety issues in laboratory settings.
The interlock system, which prevents unsafe operations, isn't wired redundantly. This means a single fault could disable the safety features, potentially causing the system to malfunction during use. The hazard is specific to laboratory environments where precise imaging techniques are performed.
Laboratory users who own or operate the DeltaVision OMX SR Imaging System model 29115476 are most at risk. The system is used for advanced imaging techniques on biological samples.
Check for the model number 29115476 on the DeltaVision OMX SR Imaging System. The system was sold with serial numbers ranging from OM20072 to OM40122.
Reach out to GE Healthcare Biosciences for specific instructions on how to handle the recalled system.
This recall specifically affects the DeltaVision OMX SR Imaging System model 29115476 with serial numbers from OM20072 to OM40122.
Contact GE Healthcare Biosciences for specific instructions on how to handle the recalled system.
Check for the model number 29115476 and serial numbers between OM20072 and OM40122 on your DeltaVision OMX SR Imaging System.
We’ve drafted a message you can send GE Healthcare Biosciences to request your refund or repair — edit it as you like.
Subject: Recall Z-0388-2019 — GE Healthcare Biosciences GE Healthcare Biosciences Hello, I own a GE Healthcare Biosciences that is covered by recall Z-0388-2019 from GE Healthcare Biosciences. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
