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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 79360

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
February 20, 2018
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Deerfield Imaging, Inc.

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

2 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 2

IMRIS ORT100 Table, Part Number 110470-000

Z-0975-2018
Recall number
Z-0975-2018
Initiated
February 20, 2018
Classification
Class II
Status
Terminated
Recalling firm
Deerfield Imaging, Inc.
Quantity
15 tables

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The rotational locking mechanisms on the ORT 100/ T2X tables can become disengaged or unlocked while in use which could potentially result in unintended movement of the table.

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

The rotational locking mechanisms on the ORT 100/ T2X tables can become disengaged or unlocked while in use which could potentially result in unintended movement of the table.

Code information

Serial Numbers: 10002341, 10003629, 10003801, 10002654, 10002795, 10002796, 10002847, 10003830, 10003243, 10002848, 10003241, 10005651, 10007348, 10007424, 10006886

Distribution pattern

US, Canada, Australia, China, Qatar

device · product 2 of 2

IMRIS T2X Table, Part Number 109682-600

Z-0976-2018
Recall number
Z-0976-2018
Initiated
February 20, 2018
Classification
Class II
Status
Terminated
Recalling firm
Deerfield Imaging, Inc.
Quantity
16 tables

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The rotational locking mechanisms on the ORT 100/ T2X tables can become disengaged or unlocked while in use which could potentially result in unintended movement of the table.

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

The rotational locking mechanisms on the ORT 100/ T2X tables can become disengaged or unlocked while in use which could potentially result in unintended movement of the table.

Code information

Serial Numbers: 10000239, 10001306, 10000983, 10000982, 10000233, 10001119, 10001192, 10002375, 10003623, 10003623, 05 002, 10003634, 10001118, 10001188, 10001340, 10003638

Distribution pattern

US, Canada, Australia, China, Qatar