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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 81454

1 recalled-product record grouped only because every row carries this exact official event ID.

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Event summary

Timeline bucket
September 10, 2018
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
GE Healthcare Biosciences

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 1

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.

Z-0388-2019
Recall number
Z-0388-2019
Initiated
September 10, 2018
Classification
Class II
Status
Terminated
Recalling firm
GE Healthcare Biosciences
Quantity
39

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Non-conformance with the DeltaVision OMX SR, the interlocks are not wired in a redundant fashion to make the interlock system single-fault tolerant.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Device Design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Non-conformance with the DeltaVision OMX SR, the interlocks are not wired in a redundant fashion to make the interlock system single-fault tolerant.

Code information

System Serial number OM20072 - OM40122

Distribution pattern

Worldwide - US Nationwide Distribution