Exact FDA event identifier

Event 89050

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

Open FDA event record

Event summary

Timeline bucket: October 26, 2021
Product types: Device
Classifications: Class II
Statuses: Ongoing
Recalling firm wording: MAX LUX CORP

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

The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range with an intended use of disinfecting surfaces.

Z-0246-2022

Recall number: Z-0246-2022
Initiated: October 26, 2021
Classification: Class II
Status: Ongoing
Recalling firm: MAX LUX CORP
Quantity: 9900 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Excessive ultraviolet-C radiation

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

Excessive ultraviolet-C radiation

Code information

Safe-T Lite

Distribution pattern

US Nationwide Distribution