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

biotene PBF Toothpaste

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 PBF Toothpaste (Plaque-Biofilm Loosening Formula), a) 4.3 oz. (121.9 g) tubes, (NDC 0135-0559-01), biotene¿ PBF Paste, b) 4.5 oz.(127.6 g) tubes, (NDC 0135-0490-02), Manufactured by Oratech, South Jordan, UTAH 84095, Distributed by GlaxoSmithKline, Consumer Healthcare, L.P., Moon Township, PA 15108

Affected NDCs 0135-0490-02 0135-0559-01

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

Recalling firm
GlaxoSmithkline Consmer Healthcare
NDC code
0135-0559-01
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1320-2015 · 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