CLASS II Drug recall · Reported 4 Nov 2015 · FDA Enforcement Report

Testosterone, Pellet, 50 mg recalled by JD & SN Inc

JD & SN Inc is recalling Testosterone, Pellet, 50 mg, distributed nationwide in the US. The recall was initiated on 24 Jul 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codest12292014@30, t11202014@11, t10132014@24, t09042014@30, t08252014@23, t06292015@23, t06252015@16, t06052015@8, t05162014@7, t05072015@11, t04302015@14, t03102015@5, t03052015@8, t03032015@33, t02182015@29, t01092015@2.
Quantity recalled16 pellets

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-0135-2016
FDA event ID
71806
Recalling firm
JD & SN Inc, Moses Lake, WA
Classification
Class II
Status
Terminated
Recall initiated
24 Jul 2015
FDA classified
27 Oct 2015
Reported
4 Nov 2015
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Sterility

Timeline

24 Jul 2015Recall initiated by company
27 Oct 2015Classified by FDA+95 days
4 Nov 2015Published in enforcement report+8 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; all sterile human compounded drugs within expiry

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, Pellet, 50 mg, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Is Testosterone, Pellet, 50 mg recalled?

Yes. JD & SN Inc recalled Testosterone, Pellet, 50 mg on 24 Jul 2015. The recall is Class II and its status is Terminated. Recall number D-0135-2016.

Why was it recalled?

Lack of Assurance of Sterility; all sterile human compounded drugs within expiry

Which lots are affected?

t12292014@30, t11202014@11, t10132014@24, t09042014@30, t08252014@23, t06292015@23, t06252015@16, t06052015@8, t05162014@7, t05072015@11, t04302015@14, t03102015@5, t03052015@8, t03032015@33, t02182015@29, t01092015@2.

Where was it sold?

Nationwide

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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