Drug recall
Ramipril Capsules, USP, 1.25 mg, 30-count bottle, Rx only, Manufactured by: Arrow Pharm (Malta) Ltd…
FDA recall event 75042 · Class III · Actavis Laboratories, FL, Inc.
Key facts
| Event ID | 75042 |
|---|---|
| Recall numbers | D-0118-2017 |
| Recalling firm | Actavis Laboratories, FL, Inc. |
| Product type | Drugs |
| Products | Ramipril Capsules, USP, 1.25 mg, 30-count bottle, Rx only, Manufactured by: Arrow Pharm (Malta) Ltd., Birzebbugia, BBG3000, Malta; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054, NDC… |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Labeling: Incorrect or Missing Lot And/or Exp Date: Bottles labeled with the incorrect expiration date of 03/18 rather than 09/17. |
| Initiation date | Aug 30, 2016 |
| Report date | Nov 9, 2016 |
| City | Davie |
| State | FL |
| Country | United States |
| FEI number | 3003194604 |
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: