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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 94533

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

Open FDA event record

Event summary

Timeline bucket
April 16, 2024
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Reflexion Medical, 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

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

RefleXion X1 Radiotherapy System Model RXM1000 Software version 2.1.19-3 Radiation therapy system is a device that combines the functionality of an emission computed tomography detection system and a linear accelerator.

Z-1933-2024
Recall number
Z-1933-2024
Initiated
April 16, 2024
Classification
Class II
Status
Ongoing
Recalling firm
Reflexion Medical, Inc.
Quantity
7 systems

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
A potential dose error exists for patients treated with an out of session SCINTIX partial fraction.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

A potential dose error exists for patients treated with an out of session SCINTIX partial fraction.

Code information

Model Number: RXM1000 UDI Codes that includes system serial numbers: (01)00860003983812(11)230504(21)X11001 (01)00860003983812(11)230518(21)X11002 (01)00860003983812(11)230505(21)X11003 (01)00860003983812(11)230530(21)X11004 (01)00860003983812(11)230811(21)X11006 (01)00860003983812(11)230410(21)X11007 (01)00860003983812(11)230803(21)X11008

Distribution pattern

U.S.: CA, CT, NJ, OR, PA and TX No O.U.S.