D-0886-2018 Class III Terminated
FDA drug recall D-0886-2018 was initiated by Dr. Reddy's Laboratories, Inc. on Jun 12, 2018 and is designated Class III. Reason for recall: Failed Impurities/Degradation Specifications The recall status is terminated (terminated Nov 8, 2019). Affected quantity: 55,126 bottles.
Recall Details
- Product Type
- Drugs
- Report Date
- Jun 27, 2018
- Initiation Date
- Jun 12, 2018
- Termination Date
- Nov 8, 2019
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 55,126 bottles
Product Description
Atorvastatin Calcium Tablets, 10 mg*, 90-count bottle, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409 INDIA, NDC 55111-121-90
Reason for Recall
Failed Impurities/Degradation Specifications
Distribution Pattern
Nationwide in the USA and Puerto Rico
Code Information
Lot #: T600327, Exp 07/18; T700213, T700215, Exp 04/19
Source
- Dataset
- openFDA drug recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for D-0886-2018
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026