🔍 RecallPedia

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

Class I - Dangerous
💊 Drugs Recalled: October 7, 2015 Vintage Pharmaceuticals LLC Prescription Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    T084M14A, T085M14A, T086M14A; Exp 12/16
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals
Reason for Recall:
Presence of Particulate Matter.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

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

Product Codes/Lot Numbers:

T084M14A, T085M14A, T086M14A; Exp 12/16

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-0232-2016

Related Recalls