🔍 RecallPedia

Xanax (Alprazolam) USP, CIV, 0.5 mg tablets , 10 x 10 blister cards per carton, Rx Only, Manufactured by Sandoz Inc., Princeton, NJ 08805, NDC 63739-669-10

Class I - Dangerous
💊 Drugs Recalled: September 15, 2016 Mckesson Packaging Services Prescription Drugs

What Should You Do?

  1. Check if you have this product:
    Lot #: 0111512; Exp. 08/17
  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:
Labeling: Missing Label-Primary packaging label (i.e. blister card) is blank and contains no product information (e.g. product name, strength, lot number, expiry).
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Xanax (Alprazolam) USP, CIV, 0.5 mg tablets , 10 x 10 blister cards per carton, Rx Only, Manufactured by Sandoz Inc., Princeton, NJ 08805, NDC 63739-669-10

Product Codes/Lot Numbers:

Lot #: 0111512; Exp. 08/17

Distribution:

Distributed in: CO, IL, LA, OH

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-1527-2016

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