Chronic hemodialysis catheter FDA Class 1 recall

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Intravenous products: The FDA have issued a Class 1 recall for the Arrow NextStep Antegrade Chronic Hemodialysis Catheter. These products were distributed to medical facilities and physicians in California, Delaware, Florida, Michigan, North Carolina, and Tennessee.

Class I recalls are the most serious type of recall and involve situations in which there is a reasonable probability that use of these products will cause serious adverse health consequences or death.

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