Biotene Gentle Mint Tubes recalls

The FDA has published 1 recall involving Biotene Gentle Mint Tubes since 2015. The latest was reported on 19 Aug 2015. Most were for foreign material. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.

Total recalls1since 2015

Last 12 months0reported

Class I00% of total

Ongoing0latest 19 Aug 2015

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 0 0 0May 0 0 0Aug 0 0

Severity split

Class I 0 0%Class II 1 100%Class III 0 0%

Why biotene gentle mint tubes is recalled

Foreign Material1100%

Companies

GlaxoSmithkline Consmer Healthcare1100%

By year

20151100%

All biotene gentle mint tubes recalls, newest first

1 total

Reported	Class	Recall	Company	Reason	Where
19 Aug 2015Drug	CLASS II	biotene Gentle Mint Gel tubes recalled by GlaxoSmithkline Consmer	GlaxoSmithkline Consmer Healthcare	Foreign Material	Nationwide

Should you stop taking Biotene Gentle Mint Tubes?

Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.