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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 83692

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

Open FDA event record

Event summary

Timeline bucket
September 04, 2019
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Elekta 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

Monaco RTP System, 5.40 Unity, radiation treatment planning system Product Usage: The Monaco system is used to make treatment plans for patients with prescriptions for external beam radiation therapy. The system calculates dose for photon, electron, and carbon treatment plans and displays, on-screen and in hard-copy, two- or three-dimensional radiation dose distributions inside patients for given treatment plan set-ups. The Monaco product line is intended for use in radiation treatment planning. It uses generally accepted methods for: -contouring -image manipulation -simulation -image fusion -plan optimization -QA and plan review

Z-2560-2019
Recall number
Z-2560-2019
Initiated
September 04, 2019
Classification
Class II
Status
Ongoing
Recalling firm
Elekta Inc
Quantity
30 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
It is possible that the forced electron density settings will be changed for some structures unintentionally and this can result in incorrect dose calculation.

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

It is possible that the forced electron density settings will be changed for some structures unintentionally and this can result in incorrect dose calculation.

Code information

UDI (01)00858164002190(10) 5.40.00

Distribution pattern

Worldwide Distribution - US Nationwide in the states of WI, OH, NY, OH, IN, IA, TX, and countries of Canada, China, Denmark, Germany, Greece, Hong Kong, Italy, Netherlands, Sweden, UK

device · product 2 of 2

Monaco RTP System, 5.50/5.51, radiation treatment planning system Product Usage: The Monaco system is used to make treatment plans for patients with prescriptions for external beam radiation therapy. The system calculates dose for photon, electron, and carbon treatment plans and displays, on-screen and in hard-copy, two- or three-dimensional radiation dose distributions inside patients for given treatment plan set-ups. The Monaco product line is intended for use in radiation treatment planning. It uses generally accepted methods for: -contouring -image manipulation -simulation -image fusion -plan optimization -QA and plan review

Z-2561-2019
Recall number
Z-2561-2019
Initiated
September 04, 2019
Classification
Class II
Status
Ongoing
Recalling firm
Elekta Inc
Quantity
49 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
It is possible that the forced electron density settings will be changed for some structures unintentionally and this can result in incorrect dose calculation.

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

It is possible that the forced electron density settings will be changed for some structures unintentionally and this can result in incorrect dose calculation.

Code information

UDI: (01)00858164002244(10) 5.50.00 (01)00858164002268(10) 5.51.00

Distribution pattern

Worldwide Distribution - US Nationwide in the states of WI, OH, NY, OH, IN, IA, TX, and countries of Canada, China, Denmark, Germany, Greece, Hong Kong, Italy, Netherlands, Sweden, UK

Field note

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