Mentor Texas recalls

Mentor Texas has 17 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 8 Jul 2026. 9 are still ongoing. 8 were reported in the last 12 months. The most frequent reason is device malfunction.

Total recalls17since 2014

Last 12 months8reported

Class I00% of total

Ongoing9latest 8 Jul 2026

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 0 7 0May 0 1 0Aug 0 0

Severity split

Class I 0 0%Class II 17 100%Class III 0 0%

Why mentor texas is recalled

Product types

By year

2026847%
202116%
201716%
2016529%
201516%
201416%

Ongoing mentor texas recalls

9 active

Reported	Class	Recall	Company	Reason	Where
8 Jul 2026Device	CLASS II	Syringe Luer Lok 10cc-200/box Bd recalled by Mentor Texas	Mentor Texas	Device Malfunction	CA, FL, PA
8 Apr 2026Device	CLASS II	Artoura Breast Tissue Expanders Reference Numbers recalled	Mentor Texas	Device Malfunction	Nationwide
8 Apr 2026Device	CLASS II	CPX 4 US Breast Tissue Expanders recalled by Mentor Texas, LP	Mentor Texas	Device Malfunction	Nationwide
8 Apr 2026Device	CLASS II	Artoura Breast Tissue Expanders Reference Numbers recalled	Mentor Texas	Device Malfunction	Nationwide
8 Apr 2026Device	CLASS II	CPX 4 US Breast Tissue Expanders recalled by Mentor Texas, LP	Mentor Texas	Device Malfunction	Nationwide
8 Apr 2026Device	CLASS II	CPX 4 US Breast Tissue Expanders recalled by Mentor Texas, LP	Mentor Texas	Device Malfunction	Nationwide

All mentor texas recalls, newest first

17 total

Reported	Class	Recall	Company	Reason	Where
8 Jul 2026Device	CLASS II	Syringe Luer Lok 10cc-200/box Bd recalled by Mentor Texas	Mentor Texas	Device Malfunction	CA, FL, PA
8 Apr 2026Device	CLASS II	Artoura Breast Tissue Expanders Reference Numbers recalled	Mentor Texas	Device Malfunction	Nationwide
8 Apr 2026Device	CLASS II	CPX 4 US Breast Tissue Expanders recalled by Mentor Texas, LP	Mentor Texas	Device Malfunction	Nationwide
8 Apr 2026Device	CLASS II	Artoura Breast Tissue Expanders Reference Numbers recalled	Mentor Texas	Device Malfunction	Nationwide
8 Apr 2026Device	CLASS II	CPX 4 US Breast Tissue Expanders recalled by Mentor Texas, LP	Mentor Texas	Device Malfunction	Nationwide
8 Apr 2026Device	CLASS II	CPX 4 US Breast Tissue Expanders recalled by Mentor Texas, LP	Mentor Texas	Device Malfunction	Nationwide
8 Apr 2026Device	CLASS II	CPX 4 US Breast Tissue Expanders recalled by Mentor Texas, LP	Mentor Texas	Device Malfunction	Nationwide
8 Apr 2026Device	CLASS II	Artoura Breast Tissue Expanders Reference Numbers recalled	Mentor Texas	Device Malfunction	Nationwide
22 Dec 2021Device	CLASS II	Mentor Saline-Filled Breast Implants are constructed recalled	Mentor Texas	Packaging Defects	Nationwide
17 May 2017Device	CLASS II	Mentor Smooth Round Spectrum Post- Operatively Adjustable recalled	Mentor Texas	Other	9 states
21 Sep 2016Device	CLASS II	Artoura Breast Tissue Expander 700 cc recalled by Mentor Texas, LP	Mentor Texas	Packaging Defects	Nationwide
21 Sep 2016Device	CLASS II	CPX4 Breast Tissue Expander 650 cc recalled by Mentor Texas, LP	Mentor Texas	Packaging Defects	Nationwide
14 Sep 2016Device	CLASS II	Mentor 2" Tall Height TE With Sutures 350cc PN recalled	Mentor Texas	E. coli	Nationwide
14 Sep 2016Device	CLASS II	Mentor 2" Tall Height TE With Sutures 450cc PN recalled	Mentor Texas	E. coli	Nationwide
10 Aug 2016Device	CLASS II	Mentor MemoryGel Breast Implant recalled by Mentor Texas, LP	Mentor Texas	Other	11 states
21 Jan 2015Device	CLASS II	Mentor MemoryGel Resterilizable Gel Sizer Moderate Plus recalled	Mentor Texas	Other	17 states
10 Sep 2014Device	CLASS II	EN Mentor Round High Profile Single Use Saline Breast recalled	Mentor Texas	Other	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.