Mentor Texas, LP recalls

Mentor Texas, LP has 16 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 8 Apr 2026. 8 are still ongoing. 7 were reported in the last 12 months. The most frequent reason is device malfunction.

Total recalls16since 2014

Last 12 months7reported

Class I00% of total

Ongoing8latest 8 Apr 2026

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 7Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 16 100%Class III 0 0%

Why mentor texas, lp is recalled

Product types

By year

2026744%
202116%
201716%
2016531%
201516%
201416%

Ongoing mentor texas, lp recalls

8 active

Reported	Class	Recall	Company	Reason	Where
8 Apr 2026Device	CLASS II	Artoura Breast Tissue Expanders Reference Numbers recalled	Mentor Texas, LP	Device Malfunction	Nationwide
8 Apr 2026Device	CLASS II	CPX 4 US Breast Tissue Expanders recalled by Mentor Texas, LP	Mentor Texas, LP	Device Malfunction	Nationwide
8 Apr 2026Device	CLASS II	Artoura Breast Tissue Expanders Reference Numbers recalled	Mentor Texas, LP	Device Malfunction	Nationwide
8 Apr 2026Device	CLASS II	CPX 4 US Breast Tissue Expanders recalled by Mentor Texas, LP	Mentor Texas, LP	Device Malfunction	Nationwide
8 Apr 2026Device	CLASS II	CPX 4 US Breast Tissue Expanders recalled by Mentor Texas, LP	Mentor Texas, LP	Device Malfunction	Nationwide
8 Apr 2026Device	CLASS II	CPX 4 US Breast Tissue Expanders recalled by Mentor Texas, LP	Mentor Texas, LP	Device Malfunction	Nationwide

All mentor texas, lp recalls, newest first

16 total

Reported	Class	Recall	Company	Reason	Where
8 Apr 2026Device	CLASS II	Artoura Breast Tissue Expanders Reference Numbers recalled	Mentor Texas, LP	Device Malfunction	Nationwide
8 Apr 2026Device	CLASS II	CPX 4 US Breast Tissue Expanders recalled by Mentor Texas, LP	Mentor Texas, LP	Device Malfunction	Nationwide
8 Apr 2026Device	CLASS II	Artoura Breast Tissue Expanders Reference Numbers recalled	Mentor Texas, LP	Device Malfunction	Nationwide
8 Apr 2026Device	CLASS II	CPX 4 US Breast Tissue Expanders recalled by Mentor Texas, LP	Mentor Texas, LP	Device Malfunction	Nationwide
8 Apr 2026Device	CLASS II	CPX 4 US Breast Tissue Expanders recalled by Mentor Texas, LP	Mentor Texas, LP	Device Malfunction	Nationwide
8 Apr 2026Device	CLASS II	CPX 4 US Breast Tissue Expanders recalled by Mentor Texas, LP	Mentor Texas, LP	Device Malfunction	Nationwide
8 Apr 2026Device	CLASS II	Artoura Breast Tissue Expanders Reference Numbers recalled	Mentor Texas, LP	Device Malfunction	Nationwide
22 Dec 2021Device	CLASS II	Mentor Saline-Filled Breast Implants are constructed from recalled	Mentor Texas, LP	Sterility	Nationwide
17 May 2017Device	CLASS II	Mentor Smooth Round Spectrum Post- Operatively Adjustable recalled	Mentor Texas, LP	Other	9 states
21 Sep 2016Device	CLASS II	Artoura Breast Tissue Expander 700 cc recalled by Mentor Texas, LP	Mentor Texas, LP	E. coli	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.