Nipro Renal Solutions Citric Complete Dry Citric Acid Concentrate Recall Over High Endotoxin Levels
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Nipro Renal Solutions USA, Corporation is recalling 7,770 cases of Citric Complete Dry Citric Acid Concentrate because the hemodialysis concentrates contain high endotoxin levels.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on September 22, 2026 and geographically references United States. The FDA classifies this as a Class II recall, with the stated reason "Hemodialysis concentrates contain high endotoxin levels", distributed 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.. FDA recall classes run from I (reasonable probability of serious harm) to III (unlikely to cause harm), so the class number is the fastest way to gauge severity here. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
Nipro Renal Solutions USA, Corporation initiated a voluntary recall of Citric Complete Dry Citric Acid Concentrate because the hemodialysis concentrates contain high endotoxin levels. The recall is classified as Class II and remains ongoing.
Which Products Are Affected
The affected products are Citric Complete Dry Citric Acid Concentrate, REF: DCA+200-25 and DCA+203-25. A total of 7,770 cases were distributed nationwide in the United States to the states of FL, GA, IL, MD, MI, NC, NJ, NV, OH, PA, and to the countries of Guatemala and Panama. Specific lots include: DCA+200-25: 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) The recall number is Z-3135-2026.
What You Should Do
The recall was initiated voluntarily by the firm via letter. Consumers in possession of the affected lots should follow guidance from the recalling firm regarding the products.
Why This Matters
The presence of high endotoxin levels in hemodialysis concentrates poses a potential risk of adverse health consequences that are temporary or reversible.
Source
FDA Enforcement Report, recall number Z-3135-2026
Original source: FDA Official Notice ↗
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