Pharm D Solutions Recalls Sermorelin/GHRP-2 Vials Due to Sterility Concerns
Pharm D Solutions, LLC is recalling Sermorelin/GHRP-2 9 mg/9 mg vials because they may lack sterility assurance. The recall covers 6 vials distributed nationwide.
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. According to the rubric, an FDA Class II recall involving a significant hazard such as lack of sterility assurance in an injectable drug corresponds to a severity score of 4 (Severe).
Plain-English summary
Pharm D Solutions, LLC is recalling Sermorelin/GHRP-2 9 mg/9 mg vials. The recall is being conducted because the product may lack sterility assurance. The affected product consists of 6 vials per package.
The recall includes Lot # 05082019:92 with an expiration date of 06/04/2019. The product was distributed nationwide within the United States. The manufacturer is Pharm D Solutions, LLC, located in Houston, Texas.
Consumers who have this product should stop using it and contact Pharm D Solutions, LLC at 1-844-263-6846 for instructions on how to return or dispose of the medication.
The recalled product
- Product
- Sermorelin/GHRP-2 9 mg/9 mg vials Pharm D. Solutions 1304 South Loop West, Houston, TX 77054, 1-844-263-6846
- Manufacturer
- Pharm D Solutions, LLC
- Category
- Drug — Injectable
- Hazard
- Affected units
- 6
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 (1)
- Lot #: 05082019:92 Exp. 06/04/2019
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 18 recalled by Pharm D Solutions, LLC 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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