Nipro Renal Solutions Citric Complete Dry Citric Acid Concentrate Recall Over High Endotoxin Levels

Source: FDA · United States

Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.

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 ↗

All FDA Recalls →

Nationwide notices with similar length or severity timing 8

Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.

What People Ask

What people usually ask about a notice like this one.

What is this FDA recall about?
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.
Which agency issued this alert?
This alert was issued by FDA. The original notice is available at the source link at the bottom of this article.
How is this recall classified, and why does that matter?
The FDA classifies this as a Class II recall, citing "Hemodialysis concentrates contain high endotoxin levels" as the reason. Class I is the most serious (reasonable probability of serious harm), Class II is a moderate or temporary health risk, and Class III is unlikely to cause harm.
What area is affected?
This alert affects United States. Check with FDA for the most current geographic scope.
Where can I find more FDA Recalls updates?
Browse the full FDA Recalls feed on Areazine at areazine.com/recalls/fda/ for the latest updates from FDA and other agencies.