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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 74899

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

Open FDA event record

Event summary

Timeline bucket
August 09, 2016
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Mentor Texas, LP.

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

Artoura Breast Tissue Expander 700 cc Product Usage: Tissue expanders can be used for breast reconstruction after mastectomy, correction of an underdeveloped breast, scar revision and tissue defect procedures. The devices are intended for temporary subcutaneous or sub muscular implantation and are not intended for use beyond six months.

Z-2780-2016
Recall number
Z-2780-2016
Initiated
August 09, 2016
Classification
Class II
Status
Terminated
Recalling firm
Mentor Texas, LP.
Quantity
48 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The CPX4 Tissue Expander may have been packaged in the Artoura Tissue Expander box.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Employee error

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The CPX4 Tissue Expander may have been packaged in the Artoura Tissue Expander box.

Code information

Lot 6944785

Distribution pattern

Worldwide Distribution - US Nationwide and the countries of: Germany, UK, and Belgium

device · product 2 of 2

CPX4 Breast Tissue Expander 650 cc : Product Usage: Tissue expanders can be used for breast reconstruction after mastectomy, correction of an underdeveloped breast, scar revision and tissue defect procedures. The devices are intended for temporary subcutaneous or sub muscular implantation and are not intended for use beyond six months.

Z-2781-2016
Recall number
Z-2781-2016
Initiated
August 09, 2016
Classification
Class II
Status
Terminated
Recalling firm
Mentor Texas, LP.
Quantity
30 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The CPX4 Tissue Expander may have been packaged in the Artoura Tissue Expander box.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Employee error

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

The CPX4 Tissue Expander may have been packaged in the Artoura Tissue Expander box.

Code information

Lot 6947019

Distribution pattern

Worldwide Distribution - US Nationwide and the countries of: Germany, UK, and Belgium

Field note

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