Drug recall
Pravastatin Sodium USP, tablets, 40 mg, 90-count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals…
FDA recall event 78566 · Class II · Lupin Limited
Key facts
| Event ID | 78566 |
|---|---|
| Recall numbers | D-0092-2018 |
| Recalling firm | Lupin Limited |
| Product type | Drugs |
| Products | Pravastatin Sodium USP, tablets, 40 mg, 90-count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202, NDC 68180-487-09 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Presence of foreign tablets/capsules: This product lot is being recalled due to a pharmacy complaint where one Duloxetine Delayed Release Capsule, 30mg was found in a Pravastatin Sodium Tablets USP… |
| Initiation date | Nov 17, 2017 |
| Report date | Nov 29, 2017 |
| Termination date | Mar 15, 2019 |
| City | Vasco Da Gama |
| Country | India |
| FEI number | 3004819820 |
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 · Source date: