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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 97284

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

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Event summary

Timeline bucket
February 07, 2025
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Jinan Bodor Cnc Machine Co Ltd

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

Bodor's I series laser cutting machine.

Z-2149-2025
Recall number
Z-2149-2025
Initiated
February 07, 2025
Classification
Class II
Status
Ongoing
Quantity
20

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The Bodor i Series products fail to meet certain applicable Federal standards, 21 CFR 1040.10(f)(1) and 21 CFR 1040.10(f)(2).

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Radiation Control for Health and Safety Act

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The Bodor i Series products fail to meet certain applicable Federal standards, 21 CFR 1040.10(f)(1) and 21 CFR 1040.10(f)(2).

Code information

The Accession Number is 2421628- 001.

Distribution pattern

US