Nipro Renal Soultions USA, Corporation
Complete recall history across all FDA and CPSC categories, 2 total recalls
Nipro Renal Soultions USA, Corporation appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Device Recalls (2)
FDA medical device enforcement actions by Nipro Renal Soultions USA, Corporation
| Date | Product | Reason | Class |
|---|---|---|---|
| Aug 5, 2026 | Citric Complete Dry Citric Acid Concentrate REF: DCA+200-25 & DCA+203-25 | Hemodialysis concentrates contain high endotoxin levels | Class II |
| Aug 5, 2026 | MedicaLyte Bicarbonate Powder REF: DB+201-2.1(45X) and DB+201-25 (35X, 36.... | Hemodialysis concentrates contain high endotoxin levels | Class II |
| Aug 5, 2026 | Citric Complete Liquid Citric Acid Concentrate REF: LC+200-D,LC+201, LC+22... | Hemodialysis concentrates contain high endotoxin levels | Class II |
| Aug 5, 2026 | MedicaLyte Liquid Bicarbonate Concentrate REF: BC-100 and BC+201 | Hemodialysis concentrates contain high endotoxin levels | Class II |
| Apr 11, 2025 | MedicaLyte Liquid Bicarbonate Concentrate. Model Numbers: BC+201 (45X), BC+10... | Potential for the presence of visible foreign matter. | Class I |
| Nov 22, 2024 | Citric Complete - Dry Citric Acid Concentrate Model Number: DCA+225-25 | The outer case is mislabeled as 3.0 K, 2.0 Ca instead of 2.0 K, 3.0 Ca. | Class II |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious, there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious, the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
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