FDA Recalls Sermorelin Injectable Solution Due to Sterility Concerns
FDA is recalling Sermorelin/GHRP-6/GHRP-2 injectable solution from Moses Lake Professional Pharmacy due to 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 hazard involves a lack of assurance of sterility in an injectable drug, which poses a significant risk of infection or serious injury.
Plain-English summary
The U.S. Food and Drug Administration (FDA) is recalling Sermorelin/GHRP-6/GHRP-2, Injectable Solution, 4.5/5.4/5.4MG/9ML, 9mL syringe, manufactured by JD & SN Inc., dba Moses Lake Professional Pharmacy. The recall involves 5 syringes distributed nationwide. The specific reason for the recall is a lack of assurance of sterility for all sterile human compounded drugs within their expiry dates.
This recall is classified as Class II by the FDA. Consumers who have this product should stop using it and contact their healthcare provider or the recalling firm for further instructions. The product is prescription-only, so patients should consult their prescriber regarding alternative treatments or next steps.
The recalled product
- Product
- SERMORELIN/GHRP-6/GHRP-2, Injectable Solution, 4.5/5.4/5.4MG/9ML, 9mL 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 Solution
- 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 (5)
- t04162015@33
- t05112015@19
- t05282015@2
- t07062015@7
- t07092015@43.
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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