D-1363-2014 Class II Terminated
FDA drug recall D-1363-2014 was initiated by Legacy Pharmaceutical Packaging on Apr 9, 2014 and is designated Class II. Reason for recall: Correct Labeled Product Miscart/Mispack: some cartons labeled as Pantoprazole Sodium Delayed-Release may contain correctly labeled blister cards of Lorazepam tablets The recall status is terminated (terminated Jan 6, 2017).
Recall Details
- Product Type
- Drugs
- Report Date
- Jun 18, 2014
- Initiation Date
- Apr 9, 2014
- Termination Date
- Jan 6, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
Product Description
Pantoprazole Sodium, Delayed-release tablets, USP, 40 mg tablets, 100 (10x10) unit dose packages, Manufactured by Dr. Reddy's Laboratories Limited, India and Distributed by Major Pharmaceuticals, Livonia, MI --- NDC 0904-6235-61
Reason for Recall
Correct Labeled Product Miscart/Mispack: some cartons labeled as Pantoprazole Sodium Delayed-Release may contain correctly labeled blister cards of Lorazepam tablets
Distribution Pattern
IN
Code Information
No lot or expiration date is displayed on this carton.
Source
- Dataset
- openFDA drug recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for D-1363-2014
- openFDA file date
- Nov 3, 2026
- Loaded by RegDataLab
- Nov 4, 2026