Official recall notice
FDA DeviceClass IINotable
FDA Recall: Citric Complete Dry Citric Acid Concentrate REF: DCA+200-25 & DCA+203-25
- Recall date
- 2026-09-16
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
Hemodialysis concentrates contain high endotoxin levels
Product description
Hemodialysis concentrates contain high endotoxin levels
Affected products
DCA+200-25 : Lots - NDC5E015(Exp.5/20/2027), NDC5E016(Exp.5/21/2027), NDC5E017(Exp.5/22/2027), NDC5E019(Exp.5/29/2027), NDC5E012(Exp.5/19/2027), NDC5B017(Exp.2/24/2027), NDC5C023(Exp.3/24/2027) DCA+203-25: NDC5C026(Exp.3/27/2027), NDC5L026(Exp.11/17/2027)