🔍 RecallPedia

Methotrexate Injection, USP, Preservative-Free, 1 g/40 mL (25 mg/mL), 40 mL Single Dose Vial, Rx only, Manufactured for: Sandoz Inc., Princeton, NJ 08540; Manufactured by: EBEWE Pharma Ges.m.b.H. Nfg.KG, A-4866 Unterach, AUSTRIA, NDC 66758-041-01.

Class I - Dangerous
💊 Drugs Recalled: May 20, 2013 Sandoz Incorporated Prescription Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot #: CL0996, Exp 12/13; and CJ4948, Exp 05/13
  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:
Sandoz Incorporated
Reason for Recall:
Presence of Particulate Matter: Found during examination of retention samples.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Methotrexate Injection, USP, Preservative-Free, 1 g/40 mL (25 mg/mL), 40 mL Single Dose Vial, Rx only, Manufactured for: Sandoz Inc., Princeton, NJ 08540; Manufactured by: EBEWE Pharma Ges.m.b.H. Nfg.KG, A-4866 Unterach, AUSTRIA, NDC 66758-041-01.

Product Codes/Lot Numbers:

Lot #: CL0996, Exp 12/13; and CJ4948, Exp 05/13

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-832-2013

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