PlainRecalls
FDA Drug Moderate Class II Terminated

Tadalafil Tablets, USP 5 mg, 30 count bottle, Rx Only, Manufactured for: Northstar Rx LLC Memphis, TN 38141, Manufactured by: Sun Pharmaceutical Industries Limited, India, NDC # 16714-075-01

Reported: November 17, 2021 Initiated: October 25, 2021 #D-0230-2022

Product Description

Tadalafil Tablets, USP 5 mg, 30 count bottle, Rx Only, Manufactured for: Northstar Rx LLC Memphis, TN 38141, Manufactured by: Sun Pharmaceutical Industries Limited, India, NDC # 16714-075-01

Reason for Recall

Incorrect Product Formulation: An incorrect grade of Crospovidone was used to manufacture the product.

Details

Units Affected
73,957 30-count bottles
Distribution
Distributed to one distributor who may have further distribute the product nationwide.
Location
Princeton, NJ

Frequently Asked Questions

What product was recalled?
Tadalafil Tablets, USP 5 mg, 30 count bottle, Rx Only, Manufactured for: Northstar Rx LLC Memphis, TN 38141, Manufactured by: Sun Pharmaceutical Industries Limited, India, NDC # 16714-075-01. Recalled by SUN PHARMACEUTICAL INDUSTRIES INC. Units affected: 73,957 30-count bottles.
Why was this product recalled?
Incorrect Product Formulation: An incorrect grade of Crospovidone was used to manufacture the product.
Which agency issued this recall?
This recall was issued by the FDA Drug on November 17, 2021. Severity: Moderate. Recall number: D-0230-2022.