PlainRecalls
FDA Devices Moderate Class II Ongoing

RAPIDPoint 500 Systems Wash/Waste Cartridge (4 Pack). Material Number: 10329097.

Reported: August 6, 2025 Initiated: June 26, 2025 #Z-2230-2025

Product Description

RAPIDPoint 500 Systems Wash/Waste Cartridge (4 Pack). Material Number: 10329097.

Reason for Recall

Siemens Healthcare Diagnostics is recalling the RAPIDPoint 500 Systems Wash/Waste Cartridge Lot WW/08925 due to a manufacturing error causing positive and negative bias in Ionized Calcium, Potassium, pH, Chloride, pCO2, Glucose and Lactate analytes and their derivatives. Four complaints were filed related to this event that led to Siemens Healthcare Diagnostics identifying an error in the manufacturing process and initiated corrective actions. Use of the affected device may result in errors during QC which could lead to a delay in patient treatment. If bias generated from this issue is not caught during QC erroneous results may cause temporary or medically reversible adverse health consequences to patients.

Details

Units Affected
1,477 units
Distribution
worldwide distribution - US Nationwide and the countries of Canada, Chile, Japan, Paraguay.
Location
Norwood, MA

Frequently Asked Questions

What product was recalled?
RAPIDPoint 500 Systems Wash/Waste Cartridge (4 Pack). Material Number: 10329097.. Recalled by Siemens Healthcare Diagnostics Inc. Units affected: 1,477 units.
Why was this product recalled?
Siemens Healthcare Diagnostics is recalling the RAPIDPoint 500 Systems Wash/Waste Cartridge Lot WW/08925 due to a manufacturing error causing positive and negative bias in Ionized Calcium, Potassium, pH, Chloride, pCO2, Glucose and Lactate analytes and their derivatives. Four complaints were filed related to this event that led to Siemens Healthcare Diagnostics identifying an error in the manufacturing process and initiated corrective actions. Use of the affected device may result in errors during QC which could lead to a delay in patient treatment. If bias generated from this issue is not caught during QC erroneous results may cause temporary or medically reversible adverse health consequences to patients.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 6, 2025. Severity: Moderate. Recall number: Z-2230-2025.