Why it was recalled
Lack of Assurance of Sterility.
Product description
PAP/PHEN/PGE1 30 mg/0.83mg/10mcg/mL Injection, 5 mL, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252
Lot numbers, UPCs & expiration codes
Lot #: 06122019@9, Exp. 07/28/2019
Where it was sold
ID, WA only
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-1481-2019
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Jun 26, 2019
- FDA report date
- Jul 17, 2019
- Quantity
- 5 mL
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- First Pharma Associates LLC dba Riverpoint Pharmacy
Original FDA data
Every field from FDA enforcement report D-1481-2019, exactly as published.
Show all FDA fields
- City
- Spokane
- State
- WA
- Status
- Terminated
- Country
- United States
- Event ID
- 83253
- Address
- 1802 N Monroe St
- Code information
- Lot #: 06122019@9, Exp. 07/28/2019
- Postal code
- 99205-4528
- Report date
- Jul 17, 2019
- Product type
- Drugs
- Recall number
- D-1481-2019
- Classification
- Class II
- Recalling firm
- First Pharma Associates LLC dba Riverpoint Pharmacy
- Product quantity
- 5 mL
- Termination date
- Jun 6, 2023
- Reason for recall
- Lack of Assurance of Sterility.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- PAP/PHEN/PGE1 30 mg/0.83mg/10mcg/mL Injection, 5 mL, Rx only, First Pharma Associates dba Riverpoint Pharmacy, Spokane, WA 99205, (509) 343-6252
- Distribution pattern
- ID, WA only
- Recall initiation date
- Jun 26, 2019
- Initial firm notification
- Telephone
- Center classification date
- Jul 11, 2019