Walgreens Recalls Levofloxacin Infusions Due to Sterility Concerns
Walgreens Infusion Services is recalling levofloxacin infusions in normal saline due to a 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 agency classified this as an FDA Class II recall. Per the rubric, FDA Class II recalls involving significant injury or property damage reports, or structural defects, are rated Severe. While specific injury reports are not detailed in the snippet, the lack of sterility assurance in an IV drug is a significant hazard warranting a Severe rating under the Class II criteria.
Plain-English summary
Walgreens Infusion Services is recalling levofloxacin in various strengths in normal saline. The recall was initiated because of a lack of sterility assurance in the products.
The affected products were distributed in Texas, Florida, Virginia, Georgia, Louisiana, and Mississippi. The source text indicates that all products within their expiry dates are included in this recall.
Consumers and healthcare providers should stop using the recalled levofloxacin infusions and contact their healthcare provider or the recalling firm for further instructions.
The recalled product
- Product
- Levofloxacin various strengths in normal saline
- Manufacturer
- Walgreens Infusion Services
- Category
- Drug — 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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