medical MODERATE Updated 2026-09-16

Nipro Renal Soultions USA, Corporation recalls Citric Complete Dry Citric Acid Concentrate REF: DCA+200-

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Recalled Product

Citric Complete Dry Citric Acid Concentrate REF: DCA+200-25 & DCA+203-25

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Hazard / Issue

Hemodialysis concentrates contain high endotoxin levels

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: 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)

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for Citric Complete Dry Citric →
View official government recall