Mentor Texas, LP.: 5 recalls on record
Recalls filed with 1 agency: FDA (5).
First recall on record: September 10, 2014. Most recent: July 8, 2026.
Risk classification: Class II: 5
Most recent recalls
| Date | Agency | Product | Recall number |
|---|---|---|---|
| July 8, 2026 | FDA | SYRINGE LUER LOK 10CC-200/BOX BD Product Code: 302995 Mentor Product Code: B9604 Syr…Z-2614-2026 | Z-2614-2026 |
| April 8, 2026 | FDA | Artoura Breast Tissue Expanders Reference Numbers: TEXP110RH TEXP120RH TEXP120RUH TEXP13…Z-1685-2026 | Z-1685-2026 |
| May 17, 2017 | FDA | Mentor Smooth Round SPECTRUM Post- Operatively Adjustable Saline Breast Implant, Product…Z-2070-2017 | Z-2070-2017 |
| September 21, 2016 | FDA | CPX4 Breast Tissue Expander 650 cc : Product Usage: Tissue expanders can be used for b…Z-2781-2016 | Z-2781-2016 |
| September 10, 2014 | FDA | EN MENTOR Round High Profile Single Use Saline Breast Implant Sizer Single Use Saline Bre…Z-2591-2014 | Z-2591-2014 |
Questions about this company
- How many recalls does Mentor Texas, LP. have?
- Recalert has 5 U.S. recalls on record for Mentor Texas, LP., published between September 10, 2014 and July 8, 2026.
- What was the most recent Mentor Texas, LP. recall?
- FDA recall Z-2614-2026, published July 8, 2026: SYRINGE LUER LOK 10CC-200/BOX BD Product Code: 302995 Mentor Product Code: B9604 Syringe, Piston
- Which agencies have handled Mentor Texas, LP. recalls?
- Mentor Texas, LP. appears as the recalling firm in recalls from: FDA (5).
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