Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
RxRecalls Get alerts
Class II · Moderate risk Terminated Initiated Jul 15, 2015 (11 years ago)

biotene Gentle Mint Gel

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.

Cause type: Particulate / foreign matter

Visible foreign particles - glass, metal, fibers or other material - found in the product. Particles can enter from equipment wear, containers or the process, and are dangerous in injectables. All particulate / foreign matter recalls.

What was recalled

biotene Gentle Mint Gel, 4.5 oz.(127.6 g) tubes, Manufactured by Oratech, South Jordan, UTAH 84095, Distributed by GlaxoSmithKline, Consumer Healthcare, L.P., Moon Township, PA 15108, NDC 0135-0488-01

Affected NDC 0135-0488-01

Compare with the code on your package — it is the most precise check available.

Recalling firm
GlaxoSmithkline Consmer Healthcare
NDC code
0135-0488-01
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1317-2015 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other recalls by GlaxoSmithkline Consmer Healthcare

All 2015 recalls

Other particulate / foreign matter recalls from 2015

All particulate / foreign matter recalls
Class I · High risk

Dextrose Injection

Presence of Particulate Matter: Confirmed customer compliants of finding an insect floating in the primary container of each product.

Terminated Particulate / foreign matter Baxter Healthcare Corp. NDC 0338-0719-06 D-0958-2016
Class I · High risk

0.9% Sodium Chloride Injection

Presence of Particulate Matter: Confirmed customer compliants of finding an insect floating in the primary container of each product.

Terminated Particulate / foreign matter Baxter Healthcare Corp. NDC 0338-0049-02 D-0957-2016