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PAP/PHEN/PGE1 22 mg/0.8mg/8mcg/mL Injection, 5mL vial, Rx only, First Pharma Associates dba River...

FDA Recall #D-1479-2019 — Class II — June 26, 2019

Recall #D-1479-2019 Date: June 26, 2019 Classification: Class II Status: Terminated

Product Description

PAP/PHEN/PGE1 22 mg/0.8mg/8mcg/mL Injection, 5mL vial, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252

Reason for Recall

Lack of Assurance of Sterility.

Recalling Firm

First Pharma Associates LLC dba Riverpoint Pharmacy — Spokane, WA

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Drugs

Product Quantity

5 mL

Distribution

ID, WA only

Code Information

Lot #: 06112019@32, Exp. 07/27/2019

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated

What Should You Do?

Stop using this medication immediately and contact your pharmacist or doctor. Do not flush medications down the drain. Return the product to the place of purchase for a refund or replacement.

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