Walgreens Recalls Cefepime Infusions Due to Sterility Assurance Concerns
Walgreens Infusion Services is recalling cefepime in normal saline due to lack of sterility assurance. The products were distributed in six southern 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 sterility assurance in an intravenous medication, which poses a significant risk of serious injury or infection.
Plain-English summary
Walgreens Infusion Services is recalling cefepime in various strengths in normal saline. The recall was initiated because of a lack of sterility assurance for the affected products.
The recalled products were distributed in Texas, Florida, Virginia, Georgia, Louisiana, and Mississippi. All products within their expiration dates are included in this recall.
Consumers and healthcare providers should stop using the recalled cefepime infusions and contact their healthcare provider or the recalling firm for further instructions.
The recalled product
- Product
- Cefepime various strengths in normal saline
- Manufacturer
- Walgreens Infusion Services
- Category
- Drug — Antibiotic Infusion
- Hazard
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 products within expiry.
Distribution
Part of a larger recall action
This product is one of 36 recalled by Walgreens Infusion Services 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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