Recall RadarAdbry, (tralokinumab-ldrm) injection, 300 mg/2mL, Packaged as a) 1 x Single dose Autoinjector, SAMPLE NOT FOR SALE, NDC 50222-350-91; b) 2 x Single dose Autoinjectors, NDC 50222-3…
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.
Read the official FDA notice →What to do
Stop using the product and check it against the description above. Follow the remedy on the official notice; most recalls are refunded or replaced without a receipt. If you or a family member has already been affected, keep the packaging and the lot code — they're what a claim rests on later.
Details
- Recalling company
- LEO PHARMA INC — Madison, NJ
- Severity
- Class II — moderate
- Reported
- March 4, 2026
- Quantity
- 11,407 units
- Recall number
- D-0339-2026
- Status
- Ongoing
- Source
- FDA
Where it went
Nationwide in the USA
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