🔍 RecallPedia

GLIMEPIRIDE TABLETS, USP 2 mg, a)100 count bottle, (NDC 42571-101-01), b) 500 count Bottle (NDC 42571-101-05), Rx only, Manufactured by: Micro Labs Limited, Goa-403 722, INDIA, Manufactured for: Micro Labs USA, Inc., Princeton, NJ 08540

Class I - Dangerous
💊 Drugs Recalled: October 9, 2014 Micro Labs Usa, Inc S Prescription Drugs

What Should You Do?

  1. Check if you have this product:
    GLBG001 Exp.12/14, GLBG008 Exp. 06/15
  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:
Micro Labs Usa, Inc S
Reason for Recall:
Failed Stability Specifications: Micro Labs is recalling two lots due to out of specification results during stability testing.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

GLIMEPIRIDE TABLETS, USP 2 mg, a)100 count bottle, (NDC 42571-101-01), b) 500 count Bottle (NDC 42571-101-05), Rx only, Manufactured by: Micro Labs Limited, Goa-403 722, INDIA, Manufactured for: Micro Labs USA, Inc., Princeton, NJ 08540

Product Codes/Lot Numbers:

GLBG001 Exp.12/14, GLBG008 Exp. 06/15

Distribution:

Distributed in: CT, FL, MD, MS, NY

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-0046-2015

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