PlainRecalls
FDA Drug Moderate Class II Terminated

HYDROCHLOROTHIAZIDE CAPSULES, USP, 12.5 mg, 3000 count bottles, Rx only, Manufactured for: Qualitest Pharmaceuticals, Inc., Huntsville, AL 35811, NDC: 0603-3855-93.

Reported: November 25, 2015 Initiated: October 7, 2015 #D-0232-2016

Product Description

HYDROCHLOROTHIAZIDE CAPSULES, USP, 12.5 mg, 3000 count bottles, Rx only, Manufactured for: Qualitest Pharmaceuticals, Inc., Huntsville, AL 35811, NDC: 0603-3855-93.

Reason for Recall

Presence of Particulate Matter.

Details

Units Affected
912 HDPE bottles
Distribution
Nationwide
Location
Huntsville, AL

Frequently Asked Questions

What product was recalled?
HYDROCHLOROTHIAZIDE CAPSULES, USP, 12.5 mg, 3000 count bottles, Rx only, Manufactured for: Qualitest Pharmaceuticals, Inc., Huntsville, AL 35811, NDC: 0603-3855-93.. Recalled by Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals. Units affected: 912 HDPE bottles.
Why was this product recalled?
Presence of Particulate Matter.
Which agency issued this recall?
This recall was issued by the FDA Drug on November 25, 2015. Severity: Moderate. Recall number: D-0232-2016.