FDAClass II · Medical device · Recalled July 8, 2026

SYRINGE LUER LOK 10CC-200/BOX BD Product Code recall — Mentor Texas LP

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

Class II: may cause temporary or medically reversible health consequences.

View the official FDA enforcement record (openFDA) ↗

Official recall ID: Z-2614-2026
Brand: Mentor Texas LP
Classification: Class II
Units affected: 1401 syringes
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Description

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

Affected products

SYRINGE LUER LOK 10CC-200/BOX BD Product Code

Companies & origin

Recalling firm location: Coppell, TX, United States
Firm address: 555 Airline Dr, N/A, 75019-4660

Identifying details (verbatim from the notice)

Product codes / lots: 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
Distribution: U.S.: CA, FL, and PA
Firm notified the public via: Letter
FDA event ID: 98981
Recall initiated: April 28, 2026
FDA classified: June 26, 2026
FDA report date: July 8, 2026

Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim; the linked government source is authoritative. Source last checked July 24, 2026 at 12:00 AM UTC.

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