Exact FDA event identifier

Event 86241

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

Open FDA event record

Event summary

Timeline bucket: July 27, 2020
Product types: Device
Classifications: Class II
Statuses: Ongoing
Recalling firm wording: Office Depot 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

JINYINSHAN, KN95 PROTECTIVE MASK P1, 20 pieces

Z-3024-2020

Recall number: Z-3024-2020
Initiated: July 27, 2020
Classification: Class II
Status: Ongoing
Recalling firm: Office Depot Inc
Quantity: 25,360 masks

App-derived interpretation

Foreign material or chemical contamination reason.foreign_material_chemical_contamination · v1.0.0

particulates

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Other

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Test results revealed that the KN95 masks failed to filter greater than 95% of particulates.

Code information

SKU 4555098 & 8510447

Distribution pattern

nationwide