Recall of LeadCare Plus and LeadCare Ultra Blood Lead Testing Systems

According to Republic of Lebanon Ministry of Public Health, this recall involved a device in Lebanon that was produced by Magellan Diagnostics Inc..

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

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