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Class II: temporary or reversible health riskTerminated

the Compounder Estriol Recall

ESTRIOL (E3) : ESTRADIOL (E2) (Estradiol (E2) Trit (Yellow)) : PROGEST (Progesterone US…

the Compounder · Aurora, IL

Risk level
Class II
Reported by FDA
Nov 18, 2015
Recall ID
D-0217-2016
Check your lot numberHow we source this data

Summary

the Compounder recalled Estriol starting Mar 10, 2015. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0217-2016 on Nov 18, 2015. Reason: Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination. Status: Terminated.

Why it was recalled

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

Product description

ESTRIOL (E3) : ESTRADIOL (E2) (Estradiol (E2) Trit (Yellow)) : PROGEST (Progesterone USP) : TESTO (Testosterone USP) W/V (weight/volume) 2 :0.1 : 35 : 0.5 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.

Lot numbers, UPCs & expiration codes

Lot # 01132015:27@20, Exp 7/12/2015

Where it was sold

Nationwide

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0217-2016
Classification
Class II
Status
Terminated
Recall initiated
Mar 10, 2015
FDA report date
Nov 18, 2015
Quantity
6 (10mL) syringes
Recall type
Voluntary: Firm initiated
Recalling firm
the Compounder

Original FDA data

Every field from FDA enforcement report D-0217-2016, exactly as published.

Show all FDA fields
City
Aurora
State
IL
Status
Terminated
Country
United States
Event ID
71535
Address
340 Marshall Ave Unit 100
Code information
Lot # 01132015:27@20, Exp 7/12/2015
Postal code
60506-5649
Report date
Nov 18, 2015
Product type
Drugs
Recall number
D-0217-2016
Classification
Class II
Recalling firm
the Compounder
Product quantity
6 (10mL) syringes
Termination date
May 19, 2016
Reason for recall
Recalled products were made using an active ingredient that was recalled by a supplier due to penicillin cross contamination.
Voluntary / mandated
Voluntary: Firm initiated
Product description
ESTRIOL (E3) : ESTRADIOL (E2) (Estradiol (E2) Trit (Yellow)) : PROGEST (Progesterone USP) : TESTO (Testosterone USP) W/V (weight/volume) 2 :0.1 : 35 : 0.5 MG/ML Transdermal cream, dispensed in 10 mL prefilled, amber syringes, Rx only, The Compounder, 340 Marshall Avenue Unit 100, Aurora, IL 60506.
Distribution pattern
Nationwide
Recall initiation date
Mar 10, 2015
Initial firm notification
Telephone
Center classification date
Nov 10, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0217-2016, published Nov 18, 2015. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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