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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 93672

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

Open FDA event record

Event summary

Timeline bucket
November 28, 2023
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
AtriCure, 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

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

Cryo Module Accessories Domestic CMA-OUS, Product Catalog Number A001053

Z-0927-2024
Recall number
Z-0927-2024
Initiated
November 28, 2023
Classification
Class II
Status
Ongoing
Recalling firm
AtriCure, Inc.
Quantity
35

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
AtriCure has identified certain lots of tank hose assemblies where a second-tier supplier provided incorrect tank hose assemblies. These tank hose assemblies were provided with an outer sheathing that does not have required pin perforations and the inner tube of the hose is not the correct material.

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

AtriCure has identified certain lots of tank hose assemblies where a second-tier supplier provided incorrect tank hose assemblies. These tank hose assemblies were provided with an outer sheathing that does not have required pin perforations and the inner tube of the hose is not the correct material.

Code information

UDI-DI: 10840143903038; Lot Numbers: 129673, 129674, 129882, 130314, 130750, 131614, 132669, 133672, 133673, 134270

Distribution pattern

US Nationwide. Brazil, Canada, Japan, Taiwan

device · product 2 of 2

Packaged, Tank Hose Assembly CMA-US, Product Catalog Number A001056

Z-0928-2024
Recall number
Z-0928-2024
Initiated
November 28, 2023
Classification
Class II
Status
Ongoing
Recalling firm
AtriCure, Inc.
Quantity
1

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
AtriCure has identified certain lots of tank hose assemblies where a second-tier supplier provided incorrect tank hose assemblies. These tank hose assemblies were provided with an outer sheathing that does not have required pin perforations and the inner tube of the hose is not the correct material.

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

AtriCure has identified certain lots of tank hose assemblies where a second-tier supplier provided incorrect tank hose assemblies. These tank hose assemblies were provided with an outer sheathing that does not have required pin perforations and the inner tube of the hose is not the correct material.

Code information

UDI-DI: 10840143903076; Lot Number: 129675

Distribution pattern

US Nationwide. Brazil, Canada, Japan, Taiwan

Field note

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