Papaverine/Phentolamine/Alprostadil 30 mg/0.2 mg/10 recall
Papaverine/Phentolamine/Alprostadil 30 mg/0.2 mg/10 mcg/mL Injectable, 2.5 mL Vial, Rx only, Compounded by Wise Pharmacy, Littleton, CO 80123.
Why was Papaverine/Phentolamine/Alprostadil 30 mg/0.2 mg/10 recalled?
Lack of Processing Controls
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: 6054N; 4796N, Exp 7/16/2019; 7049N, Exp 11/24/2019
- Product
- Papaverine/Phentolamine/Alprostadil 30 mg/0.2 mg/10 mcg/mL Injectable, 2.5 mL Vial, Rx only, Compounded by Wise Pharmacy, Littleton, CO 80123.
- Recalling firm
- Wise Pharmacy
- Quantity
- 84 vials
- Distribution
- CO, TX, WY
- Recall date
- August 7, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)