FDA Recalls Compounded Injectable Drug Due to Sterility Concerns
Oregon Compounding Centers is recalling Papaverine/Phentolamine/Prostaglandin injectable vials due to quality control issues affecting sterility assurance.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II and involves a lack of sterility assurance in injectable products, which poses a significant risk of serious injury or death if contaminated.
Plain-English summary
Oregon Compounding Centers, Inc. dba Creative Compounds is recalling all lots of sterile products compounded by the pharmacy that are not expired. The specific product identified is Papaverine/Phentolamine/Prostaglandin, 17.44mg/0.64mg/5.8mcg, injectable, 1.7 mL glass vial. The recall is driven by concerns associated with quality control procedures that present a potential risk to sterility assurance, which were observed during a recent FDA inspection.
The affected products were distributed in Oregon and Washington. The recall includes Lot # 20140910@42 with a discard date of 1/25/2015. The agency classification for this recall is Class II.
Consumers and healthcare providers should stop using the recalled products and contact their healthcare provider or the recalling firm for further instructions. This recall is precautionary based on the potential risk to sterility assurance identified during the inspection.
The recalled product
- Product
- PAPAVERINE/PHENTOLAMINE/PROSTAGLANDIN, 17.44mg/0.64mg/5.8mcg, injectable, 1.7 mL glass vial, RX, Creative Compounds, Wilsonville, OR 97070
- Category
- Drug — Compounded Injectable
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 (2)
- Lot #: 20140910@42
- discard date: 1/25/2015
Distribution
Part of a larger recall action
This product is one of 56 recalled by Oregon Compounding Centers, Inc. dba Creative Compounds 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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