Medical device recalls Moderate risk

Mentor Texas, LP. recalls MENTOR 2" Tall Height TE With Sutures 350cc PN: 354-9312 The MENTOR CPX4 and CPX4 with Suture Tabs Breast Tissue Expand…

Recall date
August 9, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2747-2016
FDA classification
Class II
Brand / firm
Mentor Texas, LP.
Sold / distributed
Worldwide Distribution: US (nationwide) and countries of: South Korea, Argentina, Mexico, Canada, Australia and New Zealand.

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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.

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