Drug recall
Nicotine Transdermal System, 7 mg delivered over 24 hours, 1 patch per pouch, Manufactured by: Aveva Drug…
FDA recall event 53441 · Class III · AVEVA Drug Delivery Systems, Inc.
Key facts
| Event ID | 53441 |
|---|---|
| Recall numbers | D-009-2010 |
| Recalling firm | AVEVA Drug Delivery Systems, Inc. |
| Product type | Drugs |
| Products | Nicotine Transdermal System, 7 mg delivered over 24 hours, 1 patch per pouch, Manufactured by: Aveva Drug Delivery Systems, Miramar, FL 33025, 4001080. |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Subpotent (Single Ingredient) Drug: AVEVA Drug Delivery Systems Inc. is recalling their 7mg/day Nicotine Transdermal Patch. Some units in Nicotine Transdermal System 7 mg delivered over 24 hours could… |
| Initiation date | Sep 24, 2009 |
| Termination date | Mar 23, 2010 |
| City | Miramar |
| State | FL |
| Country | United States |
| FEI number | 1000307689 |
At a glance
- 1–9 Products in this recall
- 10–99 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