Moses Lake Pharmacy Recalls Testosterone Cypionate Injection Due to Sterility Concerns
Moses Lake Professional Pharmacy is recalling Testosterone Cypionate for Subcutaneous Injection because the product lacks 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 involves a lack of assurance of sterility in an injectable drug, which poses a risk of serious injury or death from infection, meeting the criteria for a Severe rating.
Plain-English summary
JD & SN Inc., dba Moses Lake Professional Pharmacy, is recalling Testosterone Cypionate for Subcutaneous Injection, 100 mg/mL, 10 mL syringe. The recall is due to a lack of assurance of sterility in the compounded drug.
The affected product is a prescription-only injectable solution. The recall covers all sterile human compounded drugs within their expiration dates. The distribution pattern is listed as nationwide.
Consumers and healthcare providers should stop using the recalled product and contact their healthcare provider for further instructions.
The recalled product
- Product
- TESTOSTERONE CYPIONATE FOR SUBQ INJECTION, Injectable Solution, 100 mg/mL, 10mL syringe, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314
- Category
- Drug — Injectable
- Affected units
- 1
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 (2)
- t12102014@3
- t06252015@37
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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