Western Drug Recalls Hydroxocobalamin Injection Due to Sterility Concerns
Western Drug is recalling Hydroxocobalamin 1mg/mL Injection because the product lacks assurance of sterility. The recall covers three containers distributed nationwide.
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 three containers of Hydroxocobalamin 1mg/mL Injection. The recall was initiated because the product lacks assurance of sterility. The affected product is a prescription injection manufactured by Western Drug Inc. located in Springerville, Arizona.
The recall covers all lots of the product. Distribution was nationwide, specifically in Arizona, California, Georgia, New Mexico, South Carolina, South Dakota, Texas, and Utah. The agency has classified this recall as Class II.
Consumers and healthcare providers should stop using the recalled product and contact their healthcare provider or the manufacturer for further instructions. No specific lot numbers or expiration dates are provided in the source text.
The recalled product
- Product
- Hydroxocobalamin 1mg/mL Injection, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
- Manufacturer
- Western Drug
- Category
- Drug — Injection
- Affected units
- 3
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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