Recalls / Class II
Class IID-1479-2019
Product
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
- Affected lot / code info
- Lot #: 06112019@32, Exp. 07/27/2019
Why it was recalled
Lack of Assurance of Sterility.
Recalling firm
- Firm
- First Pharma Associates LLC dba Riverpoint Pharmacy
- Notification channel
- Telephone
- Type
- Voluntary: Firm initiated
- Address
- 1802 N Monroe St, Spokane, Washington 99205-4528
Distribution
- Quantity
- 5 mL
- Distribution pattern
- ID, WA only
Timeline
- Recall initiated
- 2019-06-26
- FDA classified
- 2019-07-11
- Posted by FDA
- 2019-07-17
- Terminated
- 2023-06-06
- Status
- Terminated
Source: openFDA Drug Enforcement endpoint. Recall record D-1479-2019. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.