Wise Pharmacy Recalls Papaverine, Phentolamine, and Alprostadil Injectable Vials
Wise Pharmacy is recalling 84 vials of compounded Papaverine/Phentolamine/Alprostadil injectable due to a lack of processing controls.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the source text does not report any illnesses or injuries, fitting the criteria for a moderate severity score.
Plain-English summary
Wise Pharmacy, located in Littleton, Colorado, is recalling 84 vials of Papaverine/Phentolamine/Alprostadil 30 mg/0.2 mg/10 mcg/mL Injectable. The product is a prescription-only compounded medication distributed in Colorado, Texas, and Wyoming.
The recall was initiated due to a lack of processing controls. Specific lot numbers and expiration dates are not provided in the source text.
Consumers who have this product should contact their healthcare provider or Wise Pharmacy for further instructions on how to proceed.
The recalled product
- 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.
- Manufacturer
- Wise Pharmacy
- Category
- Drug — Compounded Injectable
- Affected units
- 84
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 (5)
- Lot #: 6054N
- 4796N
- Exp 7/16/2019
- 7049N
- Exp 11/24/2019
Distribution
Part of a larger recall action
This product is one of 11 recalled by Wise 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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