CLASS II Drug recall · Reported 21 Oct 2015 · FDA Enforcement Report

Testosterone Cypionate (Complete Formula) 200 mg/mL recalled

Bedford Pharmacy is recalling Testosterone Cypionate (Complete Formula) 200 mg/mL, Injection, Bedford Pharmacy, 209, distributed in Massachusetts, New Hampshire. The recall was initiated on 22 Sep 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: 09032015@16 , Exp 10/18/2015
Quantity recalled2 vial

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-0047-2016
FDA event ID
72233
Recalling firm
Bedford Pharmacy, Bedford, NH
Classification
Class II
Status
Terminated
Recall initiated
22 Sep 2015
FDA classified
15 Oct 2015
Reported
21 Oct 2015
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Sterility

Timeline

22 Sep 2015Recall initiated by company
15 Oct 2015Classified by FDA+23 days
21 Oct 2015Published in enforcement report+6 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

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 (Complete Formula) 200 mg/mL, Injection, Bedford Pharmacy, 209 Route 101, Bedford, NH 03110, (603) 472-3919

Where it was distributed

NH, MA

MassachusettsNew Hampshire

Questions about this recall

Is Testosterone Cypionate (Complete Formula) 200 mg/mL, Injection, Bedford Pharmacy, 209 recalled?

Yes. Bedford Pharmacy recalled Testosterone Cypionate (Complete Formula) 200 mg/mL, Injection, Bedford Pharmacy, 209 on 22 Sep 2015. The recall is Class II and its status is Terminated. Recall number D-0047-2016.

Why was it recalled?

Lack of assurance of sterility

Which lots are affected?

Lot #: 09032015@16 , Exp 10/18/2015

Where was it sold?

NH, MA

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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