Class II ยท Moderate risk
Adbry
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.
National Drug Code
Is NDC 50222-0350-91 recalled?
Adbry · 1 SYRINGE, GLASS in 1 CARTON (50222-350-91) / 2 mL in 1 SYRINGE, GLASS (50222-350-90)
Yes — this exact package was recalled
1 FDA recall names the code 50222-0350-91 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
1 of these recalls is still ongoing.
- Active ingredient
- tralokinumab-ldrm
- Strength
- TRALOKINUMAB 300 mg/2mL
- Form
- Injection, Solution · Subcutaneous
- Labeler
- LEO Pharma Inc.
- Type
- Human Prescription Drug
- Product code
- 50222-0350
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 50222-0501 Taclonex 1
Free recall alerts
Know the day your medication is recalled
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