LEO Pharma recalls Adbry (tralokinumab-ldrm) injections due to wool fiber contamination in one unit from a specific lot. This may cause infection if injected. Affected units have NDC codes 50222-350-91 or 50222-350-02.
Lack of Assurance of Sterility: due to the presence of particulate matter in one unit from the lot, which lab tests have identified as wool fiber.
LEO Pharma is recalling Adbry injections that contain wool fiber, which could lead to infection if injected. This recall affects specific lots of the 300 mg/2mL injection product sold by prescription.
The recall is due to wool fiber found in one unit from a specific lot of the injection product. Lab tests identified this particulate matter, which could cause infection if injected into the body.
People who have been prescribed Adbry injections with NDC codes 50222-350-91 or 50222-350-02 are affected. Those who have already received the product are at risk of infection if the contaminated unit is used.
Check the NDC code on the product label: 50222-350-91 for single-dose autoinjectors or 50222-350-02 for two-dose autoinjectors. The product is only available by prescription and is labeled as a sample not for sale.
Look for the NDC code 50222-350-91 or 50222-350-02 on the product label to identify affected units.
The product is safe to use only if it has the correct NDC code and is not from the affected lots. Contaminated units may cause infection if injected.
Check the NDC code on the product label: 50222-350-91 for single-dose autoinjectors or 50222-350-02 for two-dose autoinjectors.
The official recall does not specify a remedy, so contact your healthcare provider for guidance on whether to use the product.
We’ve drafted a message you can send LEO Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0339-2026 — LEO Pharma LEO Pharma Hello, I own a LEO Pharma that is covered by recall D-0339-2026 from LEO Pharma. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
