Moses Lake Pharmacy Recalls Testosterone Propionate Injectable Solution
JD & SN Inc. is recalling 5 syringes of Testosterone Propionate Injectable Solution due to a lack of assurance of sterility.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II, and the rubric specifies that FDA Class II recalls involving significant risks like sterility issues are rated as Severe (4).
Plain-English summary
JD & SN Inc., dba Moses Lake Professional Pharmacy, is recalling 5 syringes of Testosterone Propionate, Injectable Solution, 100 mg/mL. The product is a prescription-only medication distributed nationwide.
The recall was initiated because of a lack of assurance of sterility. The source text indicates that all sterile human compounded drugs within the expiry date are affected by this issue.
Consumers who have this product should stop using it and contact their healthcare provider or the recalling firm for further instructions.
The recalled product
- Product
- TESTOSTERONE PROPRIONATE, Injectable Solution, 100 mg/mL, syringe size: 10mL, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
- Affected units
- 5
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (4)
- t02102015@6
- t03162015@29
- t04142015@12
- t05132015@11.
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 101 recalled by JD & SN Inc., dba Moses Lake Professional Pharmacy under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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