Drug recall
Kaletra capsules (Lopinavir/Ritonavir), Each soft gelatin capsule contains: Lopinavir 133.3mg, Ritonavir…
FDA recall event 27566 · Class II · Jam Pharmaceutical
Key facts
| Event ID | 27566 |
|---|---|
| Recall numbers | D-060-4 |
| Recalling firm | Jam Pharmaceutical |
| Product type | Drugs |
| Products | Kaletra capsules (Lopinavir/Ritonavir), Each soft gelatin capsule contains: Lopinavir 133.3mg, Ritonavir 33.3mg, 180 capsule bottles, Rx only, Abbott Laboratories, North Chicago, IL 60064 NDC… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Counterfeit : An unknown number of bottles bearing these lot numbers are counterfeit, in that they have been repackaged, relabeled and/or may contain different strengths or mixed strength tablets… |
| Initiation date | Oct 17, 2003 |
| City | Orange |
| Country | United States |
| FEI number | 3004054435 |
At a glance
- 1–9 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