D-0205-2017 Class III Terminated
FDA drug recall D-0205-2017 was initiated by Jubilant Cadista Pharmaceuticals, Inc. on Jun 13, 2016 and is designated Class III. Reason for recall: Labeling: Incorrect or Missing Lot and/or Exp Date: incorrect expiration date of 02/0218 is printed on the container label instead of the correct expiration date of 02/2018. The recall status is terminated (terminated Jul 12, 2017). Affected quantity: 1512 bottles.
Recall Details
- Product Type
- Drugs
- Report Date
- Dec 21, 2016
- Initiation Date
- Jun 13, 2016
- Termination Date
- Jul 12, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1512 bottles
Product Description
Methylprednisolone Tablets, USP, 16 mg, 50-count bottles, Rx only, Manufactured by Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, NDC 59746-003-14.
Reason for Recall
Labeling: Incorrect or Missing Lot and/or Exp Date: incorrect expiration date of 02/0218 is printed on the container label instead of the correct expiration date of 02/2018.
Distribution Pattern
Nationwide and Puerto Rico.
Code Information
Lot #: 16P0176, Exp 02/2018 but labeled incorrectly as 02/0218.
Source
- Dataset
- openFDA drug recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for D-0205-2017
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026