Beckman Coulter Inc Synchron LX Clinical Systems, Operating Software, All versions. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Synchron LX Clinical Systems, Operating Software, All versions.
Brand
Beckman Coulter Inc
Lot Codes / Batch Numbers
All Versions.
Products Sold
All Versions.
Beckman Coulter Inc is recalling Synchron LX Clinical Systems, Operating Software, All versions. due to Numeric results are erroneously accepted by the in-house information system without qualifying symbols "<" or ">". In addition, the in-house system m. Based on FDA medical device recall database.
Summary derived from FDA notice
The following details were not provided by the FDA: distribution information, corrective action details.
Reason for Recall
As stated by FDA
Numeric results are erroneously accepted by the in-house information system without qualifying symbols "<" or ">". In addition, the in-house system may interpret the results incorrectly.
Recommended Action
Per FDA guidance
Healthcare providers and patients should stop using the device and contact the manufacturer for further instructions. Report problems to FDA MedWatch.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026