PlainRecalls
FDA Drug Critical Class I Terminated

Hyoscyamine Sulfate, USP Tablets, 0.125 mg, 100-count tablets per bottle, Rx only, Manufactured for: Virtus Pharmaceuticals OPCO II, LLC., Nashville, TN 37217, NDC 76439-308-10.

Reported: December 28, 2016 Initiated: September 2, 2016 #D-0214-2017

Product Description

Hyoscyamine Sulfate, USP Tablets, 0.125 mg, 100-count tablets per bottle, Rx only, Manufactured for: Virtus Pharmaceuticals OPCO II, LLC., Nashville, TN 37217, NDC 76439-308-10.

Reason for Recall

Failed Content Uniformity Specifications: resulting in both superpotent and subpotent tablets.

Details

Units Affected
24,444 bottles
Distribution
Nationwide and Puerto Rico
Location
Nashville, TN

Frequently Asked Questions

What product was recalled?
Hyoscyamine Sulfate, USP Tablets, 0.125 mg, 100-count tablets per bottle, Rx only, Manufactured for: Virtus Pharmaceuticals OPCO II, LLC., Nashville, TN 37217, NDC 76439-308-10.. Recalled by VIRTUS PHARMACEUTICALS OPCO II L. Units affected: 24,444 bottles.
Why was this product recalled?
Failed Content Uniformity Specifications: resulting in both superpotent and subpotent tablets.
Which agency issued this recall?
This recall was issued by the FDA Drug on December 28, 2016. Severity: Critical. Recall number: D-0214-2017.