⚠ Data freshness notice: the most recent refresh of NHTSA was incomplete, so a
very recent recall may be missing. Everything shown is accurate as of the last checked time on this page —
for anything time-critical, confirm with the official sources linked below.
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
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 23, 2026 at 11:04 PM UTC.
Report a data error on this page