FDAClass II · Medical device · Recall Z-2614-2026 · Recalled July 8, 2026

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

Agency report date: July 8, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named: SYRINGE LUER LOK 10CC-200/BOX BD Product Code
Company / brand: Mentor Texas LP
Lot / serial / date codes: 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

Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

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

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

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

Affected product: SYRINGE LUER LOK 10CC-200/BOX BD Product Code recall status

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

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

Affected products

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

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

Other medical device recalls from around the same time

Abiomed REF recall — Oscor Inc.FDA · July 22, 2026
Abiomed REF recall — Oscor Inc.FDA · July 22, 2026
Medtronic Harmony Delivery Catheter System recall — Medtronic Heart Valves DivisionFDA · July 8, 2026
A M S recall — Windstone Medical Packaging, Inc.FDA · July 8, 2026
A M S recall — Windstone Medical Packaging, Inc.FDA · July 8, 2026

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

Found something wrong or missing? Report a data error.

Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 6:00 PM UTC. Record retrieved October 6, 2026 at 6:00 PM UTC.

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