Facility
NIPRO TECHNICAL SOLUTIONS, INC.
1 recall(s) on record — most severe on record: Class II.
| FDA Establishment Identifier (FEI) | 3003145976 |
|---|---|
| Establishment type | Manufacture Medical Device |
| Location | 3110 N Oakland Ste 101 MESA, AZ, US 85215 |
| Registration status | Active · expires 2026 |
| Parent company | NIPRO TECHNICAL SOLUTIONS, INC. (owner-operator 9061142) |
| Brand names | H&S Technical Services |
Devices registered here (1)
- Solution-Test Standard-Conductivity, DialysisProduct code FKH · Class II · Gastroenterology, Urology · 21 CFR 876.5820
Recalls & enforcement
- Class IIOngoing2025-12-12due to a defect associated with the conductivity values of the solution used to calibrate meters and result in the reporting of incorrect conductivity values for dialysate.
Related
Source: U.S. FDA via openFDA (device registration & enforcement). Data as of 2026-08-13. Verify this facility record at FDA →
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