FDA Drug recall D-0118-2017
Ramipril Capsules, USP, 1.25 mg, 30-count bottle, Rx only, Manufactured by: Arrow Pharm (Malta) Ltd., Birzebbugia, BBG3000, Malta
- FDA Drug
- Class III
- ongoing
- Published 2016-11-09
On 2016-11-09 the FDA classified a Class III recall of Ramipril Capsules, USP, 1.25 mg, 30-count bottle, Rx only, Manufactured by: Arrow Pharm (Malta) Ltd., Birzebbugia, BBG3000, Malta by Actavis Laboratories Fl, citing labeling: Incorrect or Missing Lot And/or Exp Date: Bottles labeled with the incorrect expiration date of 03/18 rather than 09/17.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0118-2017 |
| Classification | Class III |
| Status | ongoing |
| Initiated | 2016-08-30 |
| Published | 2016-11-09 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Actavis Laboratories Fl |
| Distribution | US |
Product
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 16252-570-30.
Reason
Labeling: Incorrect or Missing Lot And/or Exp Date: Bottles labeled with the incorrect expiration date of 03/18 rather than 09/17.
Identifiers
| code_info | Lot #: 1136091A, Incorrectly Labeled Exp: 03/18 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: ongoing.
Other recalls by Actavis Laboratories Fl
- Metformin Hydrochloride Extended-Release Tablets, 1000 mg, 60-count bottle, Rx only, Manufactured by: Actavis Laboratories FL, Inc., Fort L…
FDA Drug · Class II · 2015-10-21 · Actavis Laboratories Fl - Desmopressin Acetate Tablets, 0.1mg, 100 Count Bottles, Rx Only
FDA Drug · Class III · 2015-08-12 · Actavis Laboratories Fl - Cartia XT (diltiazem HCl extended-release capsules, USP), Once-A-Day Dosage, 300 mg, 90-count bottles, Rx only, Manufactured by: Watson Lab…
FDA Drug · Class III · 2015-04-22 · Actavis Laboratories Fl - Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75 mg/0.2 mg, 60-count bottle, Rx only
FDA Drug · Class II · 2014-12-03 · Actavis Laboratories Fl - Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 50 mg/0.2 mg, 60-count bottle, Rx only, Manufactured by: Watson Laboratories, In…
FDA Drug · Class II · 2014-10-08 · Actavis Laboratories Fl
All Actavis Laboratories Fl recalls
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0118-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.