Recall Z-0606-2024
Siemens Healthcare Diagnostics Inc · initiated October 26, 2023
Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature
Product
RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 100 -Intended for in vitro diagnostic use and is designed to provide the determination in whole blood. SMN: 10844813
Codes / lots: UDI-DI: 00630414947556 All serial numbers
Reason for recall
RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the potential to affect the Sodium (Na+) sensor to produce a negative bias that could result in serious injury due to a delayed diagnosis of hypernatremia or unnecessary intervention for hyponatremia and result in iatrogenic hypernatremia especially if the true sodium result is near the thresholds of severe alterations, as well as cause a Question Result -----? error flag for multiple electrolytes on patient samples and quality control that may cause a delay of diagnosis or treatment.
FDA-determined cause: Under Investigation by firm
Action taken
Siemens Healthineers issued Urgent Medical Device Correction POC 24-004.A.US on November 1, 2023 to US customers. Letter states reason for recall, health risk and action to take: Please review this letter with your Medical Director to determine the appropriate course of action, including for any previously generated results, if applicable. If you experience this issue, you may request a no-charge replacement or receive a credit from your local Siemens Healthineers representative. Complete and return the Field Correction Effectiveness Check Form attached to this letter within 30 days. Please retain this letter with your laboratory records and forward this letter to those who may have received this product. We apologize for the inconvenience this situation may cause. Siemens Healthineers is conducting a comprehensive evaluation with a cross-functional team to promptly resolve the issue with utmost priority. If you have any questions, please contact your Siemens Healthineers Customer Care Center or your local Siemens Healthineers technical support representative. Health Products Regulatory Authority (HPRA) has been notified by the Siemens Authorized Representative in Ireland. Local representatives for EU and non-EU regions have also been notified of this Urgent Field Safety Notice (OUS Version) and will follow local requirements for contacting their respective National Competent Authorities to advise them of the issue.
Details
- Recall number
- Z-0606-2024
- Initiated
- October 26, 2023
- Posted by FDA
- December 21, 2023
- Product code
- JIX – Calibrator, Multi-Analyte Mixture
- Quantity
- 0 cartridges US
- Distribution
- Nationwide with Worldwide Distribution to: Albania Algeria Angola Argentina Armenia Australia Austria Azerbaijan Bahrain Bangladesh Belarus Belgium Bolivia Bosnia and Herzegovina Botswana Brazil Brunei Darussalam Bulgaria Burkina Faso Cambodia Canada Chile China Colombia Congo, Republic Costa Rica C¿te dIvoire Croatia Cura¿ao Czech Republic Denmark Ecuador Egypt Estonia Fiji Finland France…
- Recalling firm
- Siemens Healthcare Diagnostics Inc, Norwood, MA
Other products in the same recall event
| Recall | Product | Initiated |
|---|---|---|
| Z-0607-2024 Class II | RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 250-Intended for in vitro…RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the potential to affect the Sodium (Na+)… | 10/26/2023Open, Classified |
| Z-0608-2024 Class II | RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 400-Intended for in vitro…RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the potential to affect the Sodium (Na+)… | 10/26/2023Open, Classified |
| Z-0609-2024 Class II | RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 750-Intended for in vitro…RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the potential to affect the Sodium (Na+)… | 10/26/2023Open, Classified |