Beckman Coulter Recalls Ion Selective Electrolyte Flow Cell

Beckman Coulter has recalled its Synchron LX Clinical Systems Ion Selective Electrolyte Flow Cell, according to a release by the FDA.

 

There may be wear of the ratio pump, build-up on the chloride electrode silver iodide and microbial contamination, apparently based on a maintenance-related issue, the FDA said. The company sent customers a Product Corrective Action letter about the issue on April 5.

 

The action is an FDA Class 1 recall, the most serious type, involving a reasonable probability that use of the product will cause serious adverse health consequences or death.

 

Read the FDA release on the Beckman Coulter recall.

 

Related Articles on FDA Recalls:

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