🔍 RecallPedia

Alprazolam Tablets, USP 0.25 mg, UD 100 Tablets (10 x 10), Rx Only, Mfg By: Sandoz, Inc., Princeton, NJ 08540 --- NDC 63739-644-10

Class I - Dangerous
💊 Drugs Recalled: July 30, 2014 Mckesson Packaging Services Prescription Drugs

What Should You Do?

  1. Check if you have this product:
    Lot 102492, exp 01/2016
  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:
Mckesson Packaging Services
Reason for Recall:
Presence of Foreign Substance; tablets may contain stainless steel metal particulates
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Alprazolam Tablets, USP 0.25 mg, UD 100 Tablets (10 x 10), Rx Only, Mfg By: Sandoz, Inc., Princeton, NJ 08540 --- NDC 63739-644-10

Product Codes/Lot Numbers:

Lot 102492, exp 01/2016

Distribution:

Distributed in: CO, OH

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-1515-2014

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