FDA Device recall Z-2326-2016
Mentor MemoryGel Breast Implant
- FDA Device
- Class II
- terminated
- Published 2016-08-10
On 2016-08-10 the FDA classified a Class II recall of Mentor MemoryGel Breast Implant by Mentor Texas, citing the box of 300cc MemoryGel Breast Implant was labeled with null manufacturing and expiration dates.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2326-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-07-01 |
| Published | 2016-08-10 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Mentor Texas |
| Distribution | CA, CO, IL, NC, NJ, NY, OH, RI, TN, TX, WI |
Product
Mentor MemoryGel Breast Implant; Indicated for females for breast augmentation and breast reconstruction.
Reason
The box of 300cc MemoryGel Breast Implant was labeled with null manufacturing and expiration dates.
Identifiers
| code_info | 7316994 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
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FDA Device · Class II · 2026-04-08 · Mentor Texas - Artoura Breast Tissue Expanders Reference Numbers: SDC-100H SDC-110H SDC-120H SDC-130H SDC-135H SDC-140H SDC-150H SDC-155H Smooth High Prof…
FDA Device · Class II · 2026-04-08 · Mentor Texas
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2326-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.