FDA recall, , Moderate risk
NIPRO Conductivity Standard Solutions
Conductivity Standard Solution has a defect that can cause incorrect conductivity values for dialysate.
Summary by Recall Canary from the FDA notice
What happened
NIPRO Technical Services, Inc. of Mesa, Arizona, recalled Conductivity Standard Solution due to a defect that can cause incorrect conductivity values for dialysate. The recall began December 12, 2025, and was added to the FDA's Enforcement Report on January 27, 2026.
The recalled solution was distributed nationwide in states including Alabama, Arkansas, Arizona, California, Delaware, Florida, Georgia, Illinois, Indiana, Kansas, Michigan, Missouri, North Carolina, North Dakota, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, and Washington. The solution is a secondary standard used for the calibration of conductivity cells together with conductivity meters.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Affected if its model number and UDI-DI are listed under that product.
A UDI-DI is the device identifier printed with the barcode on the device label.
Conductivity Standard Solution
- Model number
- 10001
- 10011
- 10021
- 10032
- 10040
- 10040c
- 10041
- UDI-DI
- 14250616
- 50250624
- 50250522
Recall details
- Company began the recall
- Sold in
U.S. Nationwide distribution in the states of Alabama, Arkansas, Arizona, California, Delaware, Florida, Georgia. Illinois, Indiana, Kansas, Michigan, Missouri, North Carolina, North Dakota, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee Texas, Utah, Virginia, and Washington.
- Company
- NIPRO Technical Services, Inc.Mesa, Arizona
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98030
- Recall number
- Z-1185-2026
- Quantity recalled
- 499 units
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
