Western Drug Recalls Tri-Mix ED Injection Due to Sterility Concerns
Western Drug is recalling 68 containers of Tri-Mix ED Injection because the product lacks assurance of sterility. The recall covers distribution in eight U.S. states.
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. The hazard involves a lack of assurance of sterility in an injectable medication, which poses a significant risk of infection or serious injury, meeting the criteria for a Severe rating.
Plain-English summary
Western Drug Inc. is recalling 68 containers of Tri-Mix ED Injection. The recall was initiated because the product lacks assurance of sterility. This is a prescription medication used for erectile dysfunction.
The affected product was distributed nationwide in the United States, specifically in Arizona, California, Georgia, New Mexico, South Carolina, South Dakota, Texas, and Utah. All lots of the product are included in this recall.
Consumers who have this product should stop using it and contact their healthcare provider or pharmacist for instructions on how to dispose of the medication or obtain a replacement.
The recalled product
- Product
- Tri-Mix ED Injection, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
- Manufacturer
- Western Drug
- Category
- Drug — Prescription Injection
- Affected units
- 68
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 (1)
- all lots
Distribution
Part of a larger recall action
This product is one of 91 recalled by Western Drug 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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