The Compounder Recalls Estradiol and Testosterone Cream Due to Penicillin Contamination
The Compounder is recalling specific lots of transdermal hormone cream because the active ingredient was contaminated with penicillin by a supplier.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II, and the presence of penicillin contamination poses a significant risk of severe allergic reactions or anaphylaxis, meeting the criteria for a Severe rating.
Plain-English summary
The Compounder is recalling 9 (5mL) syringes of ESTRIOL (E3) : ESTRADIOL (E2) : TESTO (Testosterone USP) W/V 2.0: 0.1: 0.5MG/ML Transdermal cream. The recalled product is dispensed in prefilled, amber syringes and is prescription-only. The specific lot number is 12102014:82@10, with an expiration date of 6/8/2015.
The recall was initiated because the active ingredient used to manufacture the product was recalled by a supplier due to penicillin cross-contamination. The distribution pattern for the affected units is listed as nationwide.
Consumers who have this specific product should stop using it and contact their healthcare provider or pharmacist for further instructions.
The recalled product
- Product
- ESTRIOL (E3) : ESTRADIOL (E2) (Estradiol (E2) Trit (Yellow)) : TESTO (Testosterone USP) W/V (weight/volume) 2.0: 0.1: 0.5MG/ML Transdermal cream, dispensed in 5 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.
- Manufacturer
- the Compounder
- Category
- Drug — Transdermal Cream
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- Lot # 12102014:82@10
- Exp 6/8/2015
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 47 recalled by the Compounder under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 47 products in this recall →Related recalls
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