Moses Lake Professional Pharmacy Recalls Sermorelin Injectable Solution
Moses Lake Professional Pharmacy is recalling 165 syringes of Sermorelin/GHRP-6/GHRP-2 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, which corresponds to a Severe severity score under the rubric for significant injury risks or hospitalization reports, even if specific injuries are not detailed in the provided text.
Plain-English summary
JD & SN Inc., dba Moses Lake Professional Pharmacy, is recalling 165 syringes of SERMORELIN/GHRP-6/GHRP-2, Injectable Solution, 9/5.4/5.4MG/9ML. The recall is being conducted because the agency identified a lack of assurance of sterility for all sterile human compounded drugs within their expiry dates.
The affected product is a prescription-only injectable solution distributed nationwide. The recall covers specific lots identified by codes such as t10062014@19 and t09152014@13, among others.
Consumers who have this product should stop using it and contact their healthcare provider or the pharmacy for further instructions.
The recalled product
- Product
- SERMORELIN/GHRP-6/GHRP-2, Injectable Solution, 9/5.4/5.4MG/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
- 165
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 (20)
- t10062014@19
- t09152014@13
- t08262014@1
- t08072014@20
- t05282015@28
- t03062015@14
- t02162015@26
- 12222014@3
- 11262014@6
- 11172014@4
- 11052014@3
- 10272014@7
- 10222014@23
- 10202014@20
- 10152014@5
- 10012014@17
- 09102014@3
- 08182014@9
- 07222014@31
- 06292015@10
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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