Home / Recalls / Akorn, Inc. / D-1170-2022

D-1170-2022 Class II Terminated

Recalled by Akorn, Inc. — Lake Forest, IL

FDA drug recall D-1170-2022 was initiated by Akorn, Inc. on Jun 10, 2022 and is designated Class II. Reason for recall: Defective Delivery System: Potential defect that could prevent the product from dispensing as intended. The recall status is terminated (terminated Sep 28, 2023). Affected quantity: 2,736 Bottles.

Recall Details

Product Type: Drugs
Report Date: Jul 6, 2022
Initiation Date: Jun 10, 2022
Termination Date: Sep 28, 2023
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 2,736 Bottles

Product Description

Calcipotriene Topical Solution, 0.005% (Scalp Solution), Rx only, 60 mL (2 fl. oz.) bottle, Manufactured by: HI-TECH PHARMACAL CO., INC., Amityville, N.Y. 11701. NDC: 50383-732-02

Reason for Recall

Defective Delivery System: Potential defect that could prevent the product from dispensing as intended.

Distribution Pattern

Nationwide in the U.S.

Code Information

Lot #: 378440, Exp. 07/31/2023

Source

Dataset: openFDA drug recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for D-1170-2022
openFDA file date: Oct 23, 2026
Loaded by RegDataLab: Oct 25, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

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