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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 74895

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

MENTOR 2" Tall Height TE With Sutures 350cc PN: 354-9312 The MENTOR CPX4 and CPX4 with Suture Tabs Breast Tissue Expanders are used for breast reconstruction following mastectomy and are intended for temporary subcutaneous or submuscular implantation and are not intended for use beyond six months.

Z-2747-2016
Recall number
Z-2747-2016
Initiated
August 09, 2016
Classification
Class II
Status
Terminated
Recalling firm
Mentor Texas, LP.
Quantity
65 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Tissue expander product mix found: CPX4 350cc was placed in a carton for the CPX4 450cc

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

Tissue expander product mix found: CPX4 350cc was placed in a carton for the CPX4 450cc

Code information

Lot 6981537

Distribution pattern

Worldwide Distribution: US (nationwide) and countries of: South Korea, Argentina, Mexico, Canada, Australia and New Zealand.

device · product 2 of 2

MENTOR 2" Tall Height TE With Sutures 450cc PN: 354-9313 The MENTOR CPX4 and CPX4 with Suture Tabs Breast Tissue Expanders are used for breast reconstruction following mastectomy and are intended for temporary subcutaneous or submuscular implantation and are not intended for use beyond six months.

Z-2748-2016
Recall number
Z-2748-2016
Initiated
August 09, 2016
Classification
Class II
Status
Terminated
Recalling firm
Mentor Texas, LP.
Quantity
70 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Tissue expander product mix found: CPX4 350cc was placed in a carton for the CPX4 450cc

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

Tissue expander product mix found: CPX4 350cc was placed in a carton for the CPX4 450cc

Code information

Lot 6981543

Distribution pattern

Worldwide Distribution: US (nationwide) and countries of: South Korea, Argentina, Mexico, Canada, Australia and New Zealand.