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Namix RA syringe recall escalate to Class I after FDA Intervention.
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Medline Industries recalled all lots of its Namic Rotating Adaptor (RA) syringes after identifying that the rotating adaptor mechanism could unwind during an active vascular procedure, risking blood loss, infection, and potentially fatal air embolism. The US regulator subsequently classify the event as a major recall.
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Namix RA syringe recall escalate to Class I after FDA Intervention.
by
@
Medline Industries recalled all lots of its Namic Rotating Adaptor (RA) syringes after identifying that the rotating adaptor mechanism could unwind during an active vascular procedure, risking blood loss, infection, and potentially fatal air embolism. The US regulator subsequently classify the event as a major recall.