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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 97961

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
October 29, 2025
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Copan Italia

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

2 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 2

1ml of DTT in liquid phase, in PET tube with capture cap, in bulk + sputum transfer device, for WASP* *Compatible with Copan s WASP (Walk-Away Specimen Processor for Microbiology) System

Z-0942-2026
Recall number
Z-0942-2026
Initiated
October 29, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Copan Italia
Quantity
122,850 units US

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Treatment reagent functionality in respiratory specimens liquification cannot be guaranteed.

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

Treatment reagent functionality in respiratory specimens liquification cannot be guaranteed.

Code information

UDI:0U020N.A - (01)18053326005036

Distribution pattern

US Distribution to states of: CA, CO, FL, GA, MN, MS, NH, NJ, NY, OH, PA, TN, TX, UT

device · product 2 of 2

1ml of DTT in liquid phase, in PET tube with capture cap, in bulk

Z-0943-2026
Recall number
Z-0943-2026
Initiated
October 29, 2025
Classification
Class II
Status
Ongoing
Recalling firm
Copan Italia
Quantity
122,850 units US

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Treatment reagent functionality in respiratory specimens fluidification cannot be guaranteed.

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

Treatment reagent functionality in respiratory specimens fluidification cannot be guaranteed.

Code information

UDI:0U020N.A - (01)18053326005043

Distribution pattern

US Distribution to states of: CA, CO, FL, GA, MN, MS, NH, NJ, NY, OH, PA, TN, TX, UT