Official recall notice
FDA DrugClass INotable
FDA Recall: Fresenius Kabi: Tyenne Injection 400 mg/20 mL vial
- Recall date
- 2026-08-11
- Brand
- Fresenius Kabi
- Category
- Drug
- FDA class
- Class I
Why it was recalled
Hazard
Due to Presence of Glass Particles
Product description
Due to Presence of Glass Particles
Affected products
Lot: 16UI07, Exp 08/31/2028