Western Drug Recalls Sermorelin Injection Due to Sterility Concerns
Western Drug is recalling 45 containers of Sermorelin Injection 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 an injectable drug, which poses a significant risk of infection or serious injury.
Plain-English summary
Western Drug Inc. is recalling 45 containers of Sermorelin Injection (10mg/10mL, 10mg/mL, 20mg/10mL, 9mg/9mL) because the product lacks assurance of sterility. The recall includes all lots of the prescription medication.
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 is classified as Class II by the FDA.
Consumers who have this product should stop using it and contact their healthcare provider or pharmacist for instructions on how to return or dispose of the medication.
The recalled product
- Product
- Sermorelin Injection 10mg/10mL,10mg/mL, 20mg/10mL, 9mg/9mL, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
- Manufacturer
- Western Drug
- Category
- Drug — Injectable Prescription
- Affected units
- 45
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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