Riverpoint Pharmacy Recalls PAP/PHEN/PGE1 Injection Due to Sterility Concerns
First Pharma Associates LLC dba Riverpoint Pharmacy is recalling specific lots of PAP/PHEN/PGE1 Injection 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, and the hazard involves a lack of assurance of sterility in an injectable drug, which poses a significant risk of serious injury or infection.
Plain-English summary
First Pharma Associates LLC dba Riverpoint Pharmacy is recalling PAP/PHEN/PGE1 30 mg/2mg/20mcg/mL Injection, 10mL vials. The recall is being conducted because of a lack of assurance of sterility for the product.
The affected product is identified by Lot # 06122019@16 with an expiration date of 07/27/2019. The recall is limited to distribution in Idaho and Washington. The product is prescription-only.
Consumers and healthcare providers should stop using the affected product and contact their healthcare provider or the recalling firm for further instructions.
The recalled product
- Product
- PAP/PHEN/PGE1 30 mg/2mg/20mcg/mL Injection, 10mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252
- Category
- Drug — Injectable
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 #: 06122019@16
- Exp. 07/27/2019
Distribution
Part of a larger recall action
This product is one of 18 recalled by First Pharma Associates LLC dba Riverpoint 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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