BIEST TD 50/50 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3)) W/V (weight /volume) 2.5 MG/ML transdermal cream, dispensed in 10 mL prefilled syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot # 01232015:03@14, Exp 4/23/2015
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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:
- the Compounder
- Reason for Recall:
- Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
BIEST TD 50/50 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3)) W/V (weight /volume) 2.5 MG/ML transdermal cream, dispensed in 10 mL prefilled syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.
Product Codes/Lot Numbers:
Lot # 01232015:03@14, Exp 4/23/2015
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: D-0187-2016
Related Recalls
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.