Vistide (cidofovir) Injection, 375 mg (75 mg/mL), 5 mL single-use vial, Rx only, Manufactured for: Gilead Sciences, Inc., Foster City, CA 94404, UPC 3 61958 01011 5; NDC 61958-0101-1.

Class I - Dangerous
💊 Drugs Recalled: January 31, 2013 Gilead Sciences Prescription Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot #: B120217A, Exp 05/15 - US Distribution
  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:
Gilead Sciences, Inc.
Reason for Recall:
Presence of Particulate Matter: Particulate matter was found in some vials of Vistide (cidofovir injection).
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Vistide (cidofovir) Injection, 375 mg (75 mg/mL), 5 mL single-use vial, Rx only, Manufactured for: Gilead Sciences, Inc., Foster City, CA 94404, UPC 3 61958 01011 5; NDC 61958-0101-1.

Product Codes/Lot Numbers:

Lot #: B120217A, Exp 05/15 - US Distribution

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-324-2013

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