ClearanceBrief
Recall Z-3133-2026 ยท KPO Dialysate Concentrate For Hemodialysis (Liquid Or Powder)

Nipro Renal Soultions USA, Corporation

MedicaLyte Liquid Bicarbonate Concentrate REF: BC-100 and BC+201

DateSep 10, 2026 (initiated Aug 5, 2026)
StatusOpen, Classified
ReasonHemodialysis concentrates contain high endotoxin levels
Root causeProcess control
ActionOn August 6, 2026 Nipro Medical Corporation issued a Urgent Medical Device Recall notification via Email. Nipro asked consignees to take the following actions: 1. Immediately examine your inventory for the affected product codes and lot numbers listed on the Recall response form. 2. Immediately segregate, quarantine, and discontinue use or distribution of any affected product in your possession. 3. Do not use, sell, transfer, or distribute affected products. 4. Complete the enclosed Recall Response Form within 10 business days, even if you do not have affected product on hand. 5. Contact Nip
Quantity3,286 cases
DistributionWorldwide - 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 recordOpen on fda.gov

510(k) clearances named in this recall

K012547HEMO-LYTE HEMODIALYSIS GRADE SODIUM BICARBONATE SOLUTION
Di-Chem, Inc., Jan 18, 2002