Exact FDA event identifier

Event 88941

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

Open FDA event record

Event summary

Timeline bucket: October 14, 2021
Product types: Device
Classifications: Class II
Statuses: Ongoing
Recalling firm wording: Beeken Biomedical, LLC

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

NuStat 8" x12" Trauma Pad XR Hemafiber, 5-pack. For temporary control of internal organ space bleeding REF: XR-0812-5

Z-0309-2022

Recall number: Z-0309-2022
Initiated: October 14, 2021
Classification: Class II
Status: Ongoing
Recalling firm: Beeken Biomedical, LLC
Quantity: 15 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Endotoxin levels exceeded allowable limits.

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

Endotoxin levels exceeded allowable limits.

Code information

Lot Code: 20C015 UDI: 00850392006544

Distribution pattern

US in the state of MO