biotene Gentle Mint Gel recall
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
Why was biotene Gentle Mint Gel recalled?
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot # Y2J101, Y2J111, Exp 08/15 Y3D031, Exp 02/16
- Product
- 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
- Recalling firm
- GlaxoSmithkline Consmer Healthcare
- Quantity
- 30,516 tubes
- Distribution
- Nationwide, Puerto Rico & Taiwan
- Recall date
- August 19, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)