HIGHFDA DRUG
LEO Pharma Recalls Adbry Injection Over Sterility Concerns
LEO Pharma Inc. recalled 11,407 units of Adbry injection on February 10, 2026. The recall stems from a lack of assurance of sterility due to particulate matter identified as wool fiber. Consumers should stop using the product immediately and contact their healthcare provider for guidance.
ADBRY
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