Mentor MemoryGel Breast Implant — Class II medical device recall Z-2326-2016
Terminated recall by Mentor Texas, LP., reported 2016-08-10, distributed in CA, CO, IL, NC, NJ, NY, OH, RI…. The box of 300cc MemoryGel Breast Implant was labeled with null manufacturing and expiration dates.
| Recall number | Z-2326-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mentor Texas, LP., Irving, TX, United States |
| Recall initiated | 2016-07-01 |
| Classified | 2016-08-03 |
| Reported by FDA | 2016-08-10 |
| Terminated | 2016-12-09 |
| Distributed | CA, CO, IL, NC, NJ, NY, OH, RI, TN, TX, WI |
| Quantity | 35 units |
| Reason classes | labeling |
Product
Mentor MemoryGel Breast Implant; Indicated for females for breast augmentation and breast reconstruction.
Reason for recall
The box of 300cc MemoryGel Breast Implant was labeled with null manufacturing and expiration dates.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2326-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.