CLASS II Drug recall · Reported 4 Nov 2015 · FDA Enforcement Report
Chorionic Gonadotropin Compounded, Injectable Solution per syringe recalled
JD & SN Inc is recalling Chorionic Gonadotropin Compounded, Injectable Solution per syringe, 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
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-0070-2016
- 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
- Drug class
- Injectable & IV Drugs
Timeline
| 24 Jul 2015 | Recall initiated by company | |
| 27 Oct 2015 | Classified by FDA | +95 days |
| 4 Nov 2015 | Published 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
CHORIONIC GONADOTROPIN COMPOUNDED, Injectable Solution, 500 UNITS/0.5ML per syringe, 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
Questions about this recall
Is Chorionic Gonadotropin Compounded, Injectable Solution per syringe recalled?
Yes. JD & SN Inc recalled Chorionic Gonadotropin Compounded, Injectable Solution per syringe on 24 Jul 2015. The recall is Class II and its status is Terminated. Recall number D-0070-2016.
Why was it recalled?
Lack of Assurance of Sterility; all sterile human compounded drugs within expiry
Which lots are affected?
t03272015@13 and t04292015@14
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.
More recalls from JD & SN Inc
All 101| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Methylcobalamin MDV, Injectable Solution, 5 MG/ML syringe recalled | JD & SN Inc | Sterility | Nationwide |
| Drug | CLASS II | Chorionic Gonadotropin, Injectable Solution/ mL vial recalled | JD & SN Inc | Sterility | Nationwide |
| Drug | CLASS II | Glutathione MDV, Injectable Solution, 200 mg/mL, syringe sizes recalled | JD & SN Inc | Sterility | Nationwide |
| Drug | CLASS II | Testosterone, Pellet, 70 mg recalled by JD & SN Inc | JD & SN Inc | Sterility | Nationwide |
| Drug | CLASS II | Dmps (Dimercapto-propanesulfonic NA (Single Use Only) recalled | JD & SN Inc | Sterility | Nationwide |