Acarbose Tablets, 25 mg, 100-count bottle, Rx only, Manufactured by: Arrow Pharm (Malta) Ltd., Birzebbugia BBG3000, Malta; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054; NDC 16252-523-01.
Reported: October 4, 2017 Initiated: September 5, 2017 #D-1178-2017
Product Description
Acarbose Tablets, 25 mg, 100-count bottle, Rx only, Manufactured by: Arrow Pharm (Malta) Ltd., Birzebbugia BBG3000, Malta; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054; NDC 16252-523-01.
Reason for Recall
Labeling: Incorrect or Missing Lot and/or Exp Date: An incorrect expiration date of July 2018 is printed on the product labeling rather than the correct expiration date of July 2017.
Details
- Recalling Firm
- Teva Pharmaceuticals USA
- Units Affected
- 3,275 bottles
- Distribution
- Nationwide in the USA
- Location
- North Wales, PA
Frequently Asked Questions
What product was recalled? ▼
Acarbose Tablets, 25 mg, 100-count bottle, Rx only, Manufactured by: Arrow Pharm (Malta) Ltd., Birzebbugia BBG3000, Malta; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054; NDC 16252-523-01.. Recalled by Teva Pharmaceuticals USA. Units affected: 3,275 bottles.
Why was this product recalled? ▼
Labeling: Incorrect or Missing Lot and/or Exp Date: An incorrect expiration date of July 2018 is printed on the product labeling rather than the correct expiration date of July 2017.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on October 4, 2017. Severity: Moderate. Recall number: D-1178-2017.
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