FDAClass IINovember 18, 2015

Estriol recall: Contamination

ESTRIOL (E3) 2.5MG suppositories, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

Why was Estriol recalled?

Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot # 01132015:97@2, Exp 4/13/2015

Product
ESTRIOL (E3) 2.5MG suppositories, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.
Recalling firm
the Compounder
Quantity
20 suppositories
Distribution
Nationwide
Recall date
November 18, 2015
Classification
Class II
Status
Terminated
Agency
FDA (drug)
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