Varithena (polidocanol injectable foam) Administration Pack For Use With Varithena, Rx only, Distributed by Biocompatibles, Inc. Oxford, CT 06478, NDC 60635-123-01

Class I - Dangerous
💊 Drugs Recalled: September 7, 2016 Biocompatibles U.K. Prescription Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot # 476670,476669,476659,475250; Exp 11/16
  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:
Biocompatibles U.K., Ltd.
Reason for Recall:
Defective Delivery System: Incorrect type of syringe found in commercially distributed administration pack
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Varithena (polidocanol injectable foam) Administration Pack For Use With Varithena, Rx only, Distributed by Biocompatibles, Inc. Oxford, CT 06478, NDC 60635-123-01

Product Codes/Lot Numbers:

Lot # 476670,476669,476659,475250; Exp 11/16

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-0001-2017

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