CLASS II Drug recall · Reported 9 Oct 2013 · FDA Enforcement Report
SIH-Testosterone Cypionate 200 mg/mL Injectable sterile recalled
Apothecary Shoppe is recalling SIH-Testosterone Cypionate 200 mg/mL Injectable sterile vial, The Apothecary Shoppe, 6136, distributed in Oklahoma. The recall was initiated on 6 Sep 2013 and the FDA has classified it as Class II.
Check your package
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-66241-002
- FDA event ID
- 66241
- Recalling firm
- Apothecary Shoppe, Tulsa, OK
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 6 Sep 2013
- FDA classified
- 3 Oct 2013
- Reported
- 9 Oct 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Sterility
- Drug class
- Injectable & IV Drugs
Timeline
| 6 Sep 2013 | Recall initiated by company | |
| 3 Oct 2013 | Classified by FDA | +27 days |
| 9 Oct 2013 | Published 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: concerns of sterility assurance with the pharmacy's independent testing laboratory
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
SIH-Testosterone Cypionate 200 mg/mL Injectable, 10 mL sterile vial, The Apothecary Shoppe, 6136 E. 51st St. Tulsa, OK 74135.
Where it was distributed
Oklahoma
Questions about this recall
Is SIH-Testosterone Cypionate 200 mg/mL Injectable sterile vial, The Apothecary Shoppe, 6136 recalled?
Yes. Apothecary Shoppe recalled SIH-Testosterone Cypionate 200 mg/mL Injectable sterile vial, The Apothecary Shoppe, 6136 on 6 Sep 2013. The recall is Class II and its status is Terminated. Recall number D-66241-002.
Why was it recalled?
Lack of Assurance of Sterility: concerns of sterility assurance with the pharmacy's independent testing laboratory
Which lots are affected?
Lot #s: 05132013@25, Exp 11/9/13; 08072013@4, Exp 2/3/14
Where was it sold?
Oklahoma
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.
More recalls from Apothecary Shoppe
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Estradiol 25 mg, Progesterone 25 mg/mL injectable sterile recalled | Apothecary Shoppe | Sterility | OK |