FDA Recalls TEG 5000 Fibrinogen Reagent Kits Due to Outdated Reference Ranges
Haemonetics Corporation is recalling TEG 5000 Functional Fibrinogen Reagent kits because the reference ranges in the instructions have shifted. Clinicians using these outdated ranges could misdiagnose patients or fail to provide necessary treatment.
- Product
- TEG 5000 Functional Fibrinogen Reagent, Item No. 07-034
- Category
- Medical Device
- Distribution
- Distributed nationwide