Mentor Texas, LP.: Medical Device Recall in 2016 - (Recall #: Z-2326-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Mentor MemoryGel Breast Implant; Indicated for females for breast augmentation and breast reconstruction.

Product Classification:

Class II

Date Initiated: July 1, 2016

Date Posted: August 10, 2016

Recall Number: Z-2326-2016

Event ID: 74565

Reason for Recall:

The box of 300cc MemoryGel Breast Implant was labeled with null manufacturing and expiration dates.

Status: Terminated

Product Quantity: 35 units

Code Information:

7316994

Distribution Pattern:

Distributed in the states of NY, WI, CA, TX, CO, NC, NJ, OH, TN, RI, and IL.

Voluntary or Mandated:

Voluntary: Firm initiated