CLASS II Drug recall · Reported 3 May 2017 · FDA Enforcement Report

Testosterone Cypionate 200 mg/mL recalled by Isomeric Pharmacy Solution

Isomeric Pharmacy Solution is recalling Testosterone Cypionate 200 mg/mL, Testosterone Propionate 20 mg/mL Multi-Dose Vial For, distributed nationwide in the US. The recall was initiated on 6 Apr 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #s: 09018, Exp 04/17/17; 09023, Exp 04/22/17; 09024, Exp 04/23/17; 09027, Exp 04/25/17; 09031, Exp 04/30/17; 10005, Exp 05/06/17; 10010, Exp 05/09/17; 11022, Exp 06/10/17; 11038, Exp 06/18/17; 11044, Exp 07/04/17; 12003, Exp 07/08/17; 12010, Exp 07/12/17; 12021, Exp 07/30/17.
Quantity recalled2,156 vials

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0686-2017
FDA event ID
76951
Recalling firm
Isomeric Pharmacy Solution, Salt Lake City, UT
Classification
Class II
Status
Terminated
Recall initiated
6 Apr 2017
FDA classified
26 Apr 2017
Reported
3 May 2017
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Sterility

Timeline

6 Apr 2017Recall initiated by company
26 Apr 2017Classified by FDA+20 days
3 May 2017Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

Testosterone Cypionate 200 mg/mL, Testosterone Propionate 20 mg/mL, 30 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Dr, SLC, UT 84109, Part # 1200, barcode 3 70285 12003 9.

Where it was distributed

Nationwide in the USA and Puerto Rico

Nationwide Puerto Rico

Questions about this recall

Is Testosterone Cypionate 200 mg/mL, Testosterone Propionate 20 mg/mL Multi-Dose Vial For recalled?

Yes. Isomeric Pharmacy Solution recalled Testosterone Cypionate 200 mg/mL, Testosterone Propionate 20 mg/mL Multi-Dose Vial For on 6 Apr 2017. The recall is Class II and its status is Terminated. Recall number D-0686-2017.

Why was it recalled?

Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Which lots are affected?

Lot #s: 09018, Exp 04/17/17; 09023, Exp 04/22/17; 09024, Exp 04/23/17; 09027, Exp 04/25/17; 09031, Exp 04/30/17; 10005, Exp 05/06/17; 10010, Exp 05/09/17; 11022, Exp 06/10/17; 11038, Exp 06/18/17; 11044, Exp 07/04/17; 12003, Exp 07/08/17; 12010, Exp 07/12/17; 12021, Exp 07/30/17.

Where was it sold?

Nationwide in the USA and Puerto Rico

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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