---
title: "SYRINGE LUER LOK 10CC-200/BOX BD Product Code: 302995 Mentor Product Code: B9... — FDA record Z-2614-2026 | Is It on Recall"
description: "A single lot of expired syringes were distributed due to a distribution system control failure."
url: https://isitonrecall.com/recall/fda-device-z-2614-2026-syringe-luer-lok-10cc-200-box-bd-product-code-302995-mentor-product-code-b9604-syringe-piston/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# SYRINGE LUER LOK 10CC-200/BOX BD Product Code: 302995 Mentor Product Code: B9604 Syringe, Piston — FDA record Z-2614-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Apr 28, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: SYRINGE LUER LOK 10CC-200/BOX BD Product Code: 302995 Mentor Product Code: B9604 Syringe, Piston
- **Reason**: A single lot of expired syringes were distributed due to a distribution system control failure.
- **Classification**: Class II
- **Recalling firm**: Mentor Texas LP
- **Quantity**: 1401 syringes
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2614-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2614-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | BD Product Code: 302995 Mentor Product Code: B9604 Sales Unit Box UDI-DI/GTIN code: 30382903029952 Individual Unit UDI-DI/GTIN code: 00382903029952 Lot Number: 8298877 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

U.S.: CA, FL, and PA

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [California](https://isitonrecall.com/state/california/)
- [Florida](https://isitonrecall.com/state/florida/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)

## Dates in the source

- **Report date**: Jul 8, 2026
- **Recall initiation date**: Apr 28, 2026
- **Center classification date**: Jun 26, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2614-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Mentor Texas, LP. records](https://isitonrecall.com/brand/mentor-texas-lp/)