Class II — Mentor Texas, LP.
| Recalling firm | MENTOR Texas, LP |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The box of 300cc MemoryGel Breast Implant was labeled with null manufacturing and expiration dates. |
| Product | Mentor MemoryGel Breast Implant; Indicated for females for breast augmentation and breast reconstruction. |
| Quantity | 35 units |
| Distribution | Distributed in the states of NY, WI, CA, TX, CO, NC, NJ, OH, TN, RI, and IL. |
| Initiated | 2016-07-01 |
| Classified | 2016-08-03 |
| Terminated | 2016-12-09 |
| Recall number | Z-2326-2016 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Mentor Texas, LP. (Z-2326-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/74565/
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