Western Drug Recalls Triamcinolone Acetonide Suspension Due to Sterility Concerns
Western Drug is recalling two containers of Triamcin 40mg/mL Suspension because the product lacks assurance of sterility. The recall covers distribution in eight US 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 and involves a lack of assurance of sterility in a parenteral medication, which poses a significant risk of serious injury or infection.
Plain-English summary
Western Drug Inc. is recalling two containers of Triamcin 40mg/mL Suspension, a prescription medication. The recall was initiated because the product lacks assurance of sterility.
The affected product was distributed nationwide in the United States, specifically in Arizona, California, Georgia, New Mexico, South Carolina, South Dakota, Texas, and Utah. The recall applies to all lots of the product.
Consumers and healthcare providers should stop using the recalled product and contact their pharmacist or healthcare provider for further instructions.
The recalled product
- Product
- Triamcin 40mg/mL Susp, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
- Manufacturer
- Western Drug
- Category
- Drug — Sterile Injectable
- Hazard
- Affected units
- 2
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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