D-0810-2018 Class III Terminated

Recalled by Aidarex Pharmaceuticals LLC — Corona, CA

FDA drug recall D-0810-2018 was initiated by Aidarex Pharmaceuticals LLC on April 10, 2018 and is designated Class III. Reason for recall: Presence of Foreign Tablets/Capsules The recall status is terminated (terminated December 4, 2019). Affected quantity: 450 bottles.

Recall Details

Product Type
Drugs
Report Date
May 23, 2018
Initiation Date
April 10, 2018
Termination Date
December 4, 2019
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
450 bottles

Product Description

Ferrous Sulfate 325 MG tablet; NDC 33261-0715-00

Reason for Recall

Presence of Foreign Tablets/Capsules

Distribution Pattern

Product was distributed to Florida

Code Information

NDC 33261-0715-00 Batch ID: 57909-1, exp. date 04/30/2019 57909-2, exp. date 06/30/2019