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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 92942

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

Open FDA event record

Event summary

Timeline bucket
August 09, 2023
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
O&M HALYARD, 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

FLUIDSHIELD 3 N95 Particulate Filter Respirator and Surgical Mask with SO SOFT* Lining, Orange, size small, Product Code 46827

Z-2626-2023
Recall number
Z-2626-2023
Initiated
August 09, 2023
Classification
Class II
Status
Ongoing
Recalling firm
O&M HALYARD, INC.
Quantity
41790 masks

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
One respirator sample failed a filtration efficiency test. This respirator may not provide adequate protection to the user.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Unknown

An exact joined enrichment record exists, but none supplies supported root-cause wording. This is not an FDA finding of an unknown cause.

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

One respirator sample failed a filtration efficiency test. This respirator may not provide adequate protection to the user.

Code information

UDI-DI: 20680651468271; Lot Number AM2164811

Distribution pattern

US Distribution to States of: FL, GA, IA, IL, MO, MS, NE, OK, TN, TX, WI and OUS International to country of: Columbia

Field note

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