Pharm D Solutions Recalls Sermorelin/GHRP-2 Powder Due to Sterility Concerns
Pharm D Solutions is recalling 330 vials of Sermorelin/GHRP-2 Powder because the company cannot ensure the product is sterile.
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 sterile product defect (which carries a risk of serious infection) falls under the 'Severe' category, particularly given the lack of assurance of sterility for an injectable powder.
Plain-English summary
Pharm D Solutions, LLC is recalling 330 vials of Sermorelin/GHRP-2 9 mg-6 mg Powder (NDC 69699-1728-10). The recall was initiated because the company lacks assurance of the product's sterility.
The affected product was distributed nationwide. The recall covers two specific lots: Lot 03202018:06 with a discard by date of 9/16/2018, and Lot 06112018:49 with a discard by date of 12/8/2018.
Consumers and healthcare providers should stop using the recalled product and contact Pharm D Solutions, LLC or their healthcare provider for further instructions.
The recalled product
- Product
- Sermorelin/GHRP-2 9 mg-6 mg Powder, Pharm D Solutions, Houston, Texas --- NDC 69699-1728-10
- Manufacturer
- Pharm D Solutions, LLC
- Category
- Drug — Injectable Powder
- Affected units
- 330
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)
- Lot: 03202018:06 Discard by: 9/16/2018
- 06112018:49 Discard by: 12/8/2018
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 79 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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