Device recall: MedicaLyte Liquid Bicarbonate Concentrate REF: BC-100 and BC+201
Class II FDA enforcement event 99573. Recall start date: . Status in the FDA record: Ongoing.
Reason for recall, in the words of FDA
Hemodialysis concentrates contain high endotoxin levels
Class II, in the words of FDA
a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Nipro Renal Soultions USA, Corporation started this device recall on 5 Aug 2026. The firm address in the FDA record is in Lewisberry, PA. FDA put the recall in Class II. FDA event 99573 has 4 product records. The first FDA enforcement report date is 16 Sep 2026. The record gives the status Ongoing.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
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.
Recalling firm
Nipro Renal Soultions USA, Corporation, Lewisberry, PA.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
4 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-3133-2026 | MedicaLyte Liquid Bicarbonate Concentrate REF: BC-100 and BC+201 | 3,286 cases | Class II | Ongoing | 16 Sep 2026 |
| Z-3134-2026 | MedicaLyte Bicarbonate Powder REF: DB+201-2.1(45X) and DB+201-25 (35X, 36.83X, 45X)) | 2,327 cases | Class II | Ongoing | 16 Sep 2026 |
| Z-3135-2026 | Citric Complete Dry Citric Acid Concentrate REF: DCA+200-25 & DCA+203-25 | 7,770 cases | Class II | Ongoing | 16 Sep 2026 |
| Z-3136-2026 | Citric Complete Liquid Citric Acid Concentrate REF: LC+200-D,LC+201, LC+225(45X) | 100 drums/1072 cases | Class II | Ongoing | 16 Sep 2026 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Device events that started in 2026
- 572
- Share of these events in Class II
- 87%
- Product records in this event
- 4Median of the firm: 1
- Events of the firm on the register
- 3
Other events of the firm
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 11 Apr 2025 | MedicaLyte Liquid Bicarbonate Concentrate. Model Numbers: BC+201 (45X), BC+100 36.83X. Plastic bottle packaged in corrug | Device | Class I | 1 |
| 22 Nov 2024 | Citric Complete - Dry Citric Acid Concentrate Model Number: DCA+225-25 | Device | Class II | 1 |
Official channels
- FDA enforcement report Z-3133-2026The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA MedWatchThe FDA safety reporting program for drugs and medical devices.
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Cite this page
Recall Register. FDA enforcement event 99573. https://recallregister.com/fda/ii/99573/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA device enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
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.
- What quantity of product is in FDA event 99573?
- The event has 4 product records. The first record gives this quantity:
3,286 cases
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many device recalls of 2026 have the same class?
- 87% of the 572 device events that started in 2026 are in Class II.