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.
Reported: November 9, 2016 Initiated: August 30, 2016 #D-0118-2017
Product Description
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 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.
Details
- Recalling Firm
- Actavis Laboratories, FL, Inc.
- Units Affected
- 15,984 bottles
- Distribution
- Nationwide and Puerto Rico
- Location
- Davie, FL
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Actavis Laboratories, FL, Inc.. Units affected: 15,984 bottles.
Why was this product recalled? ▼
Labeling: Incorrect or Missing Lot And/or Exp Date: Bottles labeled with the incorrect expiration date of 03/18 rather than 09/17.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on November 9, 2016. Severity: Low. Recall number: D-0118-2017.
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