# FDA recall Z-2614-2026

> **Mentor Texas LP** · Class II · device recall initiated 2026-04-28.

## Product

SYRINGE LUER LOK 10CC-200/BOX  BD Product Code: 302995  Mentor Product Code: B9604    Syringe, Piston

## Reason for recall

A single lot of expired syringes were distributed due to a distribution system control failure.

## Distribution

U.S.: CA, FL, and PA

## Key facts

- **Recall number:** Z-2614-2026
- **Recalling firm:** Mentor Texas LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-04-28
- **Report date:** 2026-07-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Coppell, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2614-2026

## Citation

> MORVS. FDA recall Z-2614-2026. Retrieved 2026-10-21 from https://api.morvs.ai/recall/Z-2614-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*