Reported Nov 18, 2015 · Terminated
BIEST TD 50/50 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3)) W/V (weight /volume) 4.0 MG/ML transdermal…
the Compounder
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: the Compounder · 340 Marshall Ave Unit 100 · Aurora, IL · 60506-5649
Is this the product you have?
- BIEST TD 50/50 (Estradiol USP Micronized (E2)/Estriol USP Micronized (E3)) W/V (weight /volume) 4.0 MG/ML transdermal cream packaged in 3mL syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.
- Lot codes and dates
Lot # 12232014:11@21Exp 6/21/2015
- Amount recalled
- 5 (3mL) syringes
This recall covers 47 products
The agency filed one notice per product. You are reading one of them; the other 46 are below.
34 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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