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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 92230

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

Open FDA event record

Event summary

Timeline bucket
April 27, 2023
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
NRT X-RAY A/S

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

Intelli-C, Right side suspended Tabletop, REF: 03400000

Z-1668-2023
Recall number
Z-1668-2023
Initiated
April 27, 2023
Classification
Class II
Status
Ongoing
Recalling firm
NRT X-RAY A/S
Quantity
32 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
There is a potential that the drive shaft in the detector up/down (IDE) movement of the X-Ray machine may break which causes the detector to move until it is stopped by the movement end-stop.

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

There is a potential that the drive shaft in the detector up/down (IDE) movement of the X-Ray machine may break which causes the detector to move until it is stopped by the movement end-stop.

Code information

UDI-DI: 05713464000527/Serial Numbers: 627004, 627007, 639001, 639002,639003, 639004, 639007, 639010, 647001, 647004, 647005, 648001, 651007, 658002, 658003, 658006, 658010, 666008, 675001, 675004, 682006, 682010

Distribution pattern

US Nationwide distribution in the states of OH, NC, KY, SC, IA, MA, WA, LA, NV, NY.

device · product 2 of 2

Intelli-C, Left side suspended Tabletop, REF: 03400010

Z-1669-2023
Recall number
Z-1669-2023
Initiated
April 27, 2023
Classification
Class II
Status
Ongoing
Recalling firm
NRT X-RAY A/S
Quantity
13 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
There is a potential that the drive shaft in the detector up/down (IDE) movement of the X-Ray machine may break which causes the detector to move until it is stopped by the movement end-stop.

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

There is a potential that the drive shaft in the detector up/down (IDE) movement of the X-Ray machine may break which causes the detector to move until it is stopped by the movement end-stop.

Code information

UDI-DI:05713464000121/Serial Numbers: 647009, 651002, 651006, 666009, 682003

Distribution pattern

US Nationwide distribution in the states of OH, NC, KY, SC, IA, MA, WA, LA, NV, NY.