Drug recall
Allegra, Fexofenadine HCL, 180MG, TAB, Mfg. Lot 1116394, Exp. 04/21/09, Mfg. AVE, Rx only, NDC 00088-1109-47…
FDA recall event 50779 · Class II, Class III · Advantage Dose LLC
Key facts
| Event ID | 50779 |
|---|---|
| Recall numbers | D-814-2009, D-815-2009, D-816-2009, D-817-2009, D-818-2009, D-819-2009, D-820-2009, D-821-2009, D-822-2009, D-823-2009, D-824-2009, D-825-2009 and 104 more |
| Recalling firm | Advantage Dose LLC |
| Product type | Drugs |
| Products | Allegra, Fexofenadine HCL, 180MG, TAB, Mfg. Lot 1116394, Exp. 04/21/09, Mfg. AVE, Rx only, NDC 00088-1109-47, Adv Dose Shreveport, LA, Aloxi, Palonosetron HCl, 0.25Mg/5ML Vial, Mfg. Lot 27004036, Exp. 02/01/10, Mfg. MGI, Rx only, Advantage Dose - Shreveport, LA, Altace, Ramipril, 1.25MG CAP, Mfg. Lot 51139, Exp. 04/22/09, Mfg. MNR, Rx only, Adv Dose Shrvprt, LA, Aminophylline, 200MG TAB, Mfg. Lot 63687A, Exp. 04/15/09, Mfg W-W, Rx only, NDC 00143-1025-01, Adv Dose Shrvprt, LA, Arimmidex, Anastrozole, 1MG TABLET, Mfg. Lot PC0089, Exp. 04/25/09, Mfg. A/Z, Rx only, NDC 00310-0201-30, Adv Dose Shreveport, LA and 110 more |
| Classification | Class II, Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | lack of stability data to support product expiry, Not in conformance with cGMP |
| Initiation date | Nov 26, 2008 |
| Termination date | Oct 5, 2009 |
| City | Shreveport |
| State | LA |
| Country | United States |
| FEI number | 3006586297 |
At a glance
- 100–999 Products in this recall
- 1–9 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