PlainRecalls
FDA Drug Moderate Class II Terminated

Venlafaxine Tablets, USP 50 mg*, 100 Tablets Manufactured for Northstar Rx LLC Memphis, TN 38141 Manufactured by: ALKALOIDA Chemical Company Zrt. 4440 Tiszavasvari, Kabay Janos u.29.Hungary. Product of India NDC 16714-657-01

Reported: August 18, 2021 Initiated: July 29, 2021 #D-0703-2021

Product Description

Venlafaxine Tablets, USP 50 mg*, 100 Tablets Manufactured for Northstar Rx LLC Memphis, TN 38141 Manufactured by: ALKALOIDA Chemical Company Zrt. 4440 Tiszavasvari, Kabay Janos u.29.Hungary. Product of India NDC 16714-657-01

Reason for Recall

Presence of Forein Tablets/Capsules; Venlafaxine Tablets, USP 37.5 mg found in bottles labeled as Venlafaxine Tablets, USP, 50 mg

Details

Units Affected
2856 bottles
Distribution
Northstar Distribution Center 4853 Crumpler Rd. Memphis, TN 38141
Location
Princeton, NJ

Frequently Asked Questions

What product was recalled?
Venlafaxine Tablets, USP 50 mg*, 100 Tablets Manufactured for Northstar Rx LLC Memphis, TN 38141 Manufactured by: ALKALOIDA Chemical Company Zrt. 4440 Tiszavasvari, Kabay Janos u.29.Hungary. Product of India NDC 16714-657-01. Recalled by SUN PHARMACEUTICAL INDUSTRIES INC. Units affected: 2856 bottles.
Why was this product recalled?
Presence of Forein Tablets/Capsules; Venlafaxine Tablets, USP 37.5 mg found in bottles labeled as Venlafaxine Tablets, USP, 50 mg
Which agency issued this recall?
This recall was issued by the FDA Drug on August 18, 2021. Severity: Moderate. Recall number: D-0703-2021.