FDA · Medical devices ·
Citric Complete Dry Citric Acid Concentrate REF: DCA+200-25 & DCA+203-25 recall
Nipro Renal Soultions USA, Corporation recalled Citric Complete Dry Citric Acid Concentrate REF: DCA+200-25 & DCA+203-25 on September 16, 2026 because of hemodialysis concentrates contain high endotoxin levels. It was sold nationwide.
Why it was recalled
Hemodialysis concentrates contain high endotoxin levels
What's recalled
Citric Complete Dry Citric Acid Concentrate REF: DCA+200-25 & DCA+203-25
Quantity: 7,770 cases
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Nipro Renal Soultions USA, Corporation, Lewisberry, PA
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
Worldwide - US Nationwide distribution in the states of FL, GA, IL, MD, MI, NC, NJ, NV, OH, PA, and the countries of Guatemala and Panama. - Status
- Ongoing
- Recall number
- Z-3135-2026
- Source
- U.S. Food and Drug Administration
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