Drug recall
Aquafresh Fluoride Toothpaste Triple Protection, 2 Tubes-Net Wt 8.2oz (232.4g) each; Glaxo Smith Line Consumer…
FDA recall event 58757 · Class III · GlaxoSmithKline Consumer Healthcare LP
Key facts
| Event ID | 58757 |
|---|---|
| Recall numbers | D-777-2011 |
| Recalling firm | GlaxoSmithKline Consumer Healthcare LP |
| Product type | Drugs |
| Products | Aquafresh Fluoride Toothpaste Triple Protection, 2 Tubes-Net Wt 8.2oz (232.4g) each; Glaxo Smith Line Consumer Healthcare LP Moon Township, PA 15108, Made in the USA ; EXP11/2012 (L)0K0; Case UPC… |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Incorrect product formulation; OTC toothpaste contain bubble gum flavoring instead of mint flavoring. |
| Initiation date | Apr 11, 2011 |
| Termination date | Jan 10, 2012 |
| City | Parsippany |
| State | NJ |
| Country | United States |
| FEI number | 3008327576 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports